FCC ID: IFU380100 ISM 900 Vitality GlowPack

by: NantWorks latest update: 2012-06-08 model: 380100

One grant has been issued under this FCC ID on 06/08/2012 (this is the only release in 2012 for this grantee). Public details available include frequency information, manuals, and internal & external photos. some products also feature user submitted or linked password defaults, drivers, instructions, troubleshooting guides, & warrantee terms.

permalink for this FCC identifier

search for: Repair details

from iFixIt

Trade-in? Recycling locations

eg for Slack usage

all	frequencies		exhibits	applications
		manual

all exhibits 10
1 ~ 2012-06-08 10

app s				submitted / available
1	GlowPack User Manual Rev02	Users Manual	pdf	223.65 KiB	August 06 2012 / April 12 2012
1		Cover Letter(s)	pdf		August 06 2012
1		External Photos	pdf		August 06 2012 / April 12 2012
1		Test Setup Photos	pdf		August 06 2012 / April 12 2012
1		ID Label/Location Info	pdf		August 06 2012
1		Cover Letter(s)	pdf		August 06 2012
1		RF Exposure Info	pdf		August 06 2012
1		Test Report	pdf		August 06 2012
1		Internal Photos	pdf		August 06 2012 / April 12 2012
1		Cover Letter(s)	pdf		August 06 2012

exhibit
download
text

GlowPack User Manual Rev02

Users Manual

pdf

223.65 KiB

August 06 2012 / April 12 2012

GlowPack User Manual NantWorks Confidential and Proprietary. Restricted Distribution. This document should not be used without the consent of NantWorks. The recipient of this document must respect the propriety and keep the confidentiality of the information included. The latest revision of this document may be obtained by contacting NantWorks LLC. NantWorks Confidential and Proprietary Rev. 02 pg. 1 NantWorks LLC Del Mar Office 12230 El Camino Real, Suite 400 San Diego, CA 92130 The information disclosed in this document is proprietary to NantWorks., and should not be used or disclosed to any unauthorized persons without consent of NantWorks. The recipient of this document should respect the security and propriety and keep the confidentiality of the information included. The latest revision of this document may be obtained by contacting NantWorks. By accepting this material the recipient agrees that this material and the information contained therein is to be held in confidence and in trust, and will not be used, copied, reproduced in whole or in part, nor its contents revealed in any manner to others without the clear written permission from NantWorks LLC. NantWorks reserves the right to make changes to the product(s) or information contained herein without notice. No liability is assumed for any damages arising directly or indirectly by their use or application. The information provided in this document is provided on an as is basis. GlowPack User Manual Rev. 01 April 18, 2012 NantWorks Confidential and Proprietary Rev. 02 pg. 2 Contents 1 Introduction 2 Vitality Products Overview 3 Regulatory Approvals 4 GlowPack Function Description Figures Figure 1. The Vitality product family description Figure 2. GlowPack device and how it works with Vitality Reminder Light Figure 3. A sample server interface of how the medical dose time could be configured. Revision History Revision 01 02 Description of Revision Initial Release Revision after feedback Date April 18, 2012 May 10, 2012 NantWorks Confidential and Proprietary Rev. 02 pg. 3 1 Introduction This document describes the general functions of Vitality products family, and how the GlowPack product is added to this family. It also provides the basic instructions of how the product is used, including the hardware and software interfaces. 2 Vitality Products Overview The Vitality product family includes personal Reminder Light and GlowCap units. The GlowCap units are filled with medicine from Pharmacy. The dose time is pre-programmed via a web interface to the Vitality servers by the doctors/nurses/medical specialists. When the Reminder Light is inserted into the power outlet at home, it will automatically search for a cellular network signal, connect to Vitality servers, and download the latest medical dose information. When it is time for a dose, the GlowCap device will activate to remind the patient to take the medicine. Patients can receive additional reminders via a phone call and/or text message to the patients mobile phone. Currently, both Reminder Light and GlowCap devices have been FCC proved. The GlowPack device is a device which can be added to the Vitality family product. The usage instructions for the GlowPack are provided in Chapter 4. NantWorks Confidential and Proprietary Rev. 02 pg. 4 Figure 1. The Vitality product family description 3 Regulatory Approvals The GlowPack is currently designed to meet regulations for use in the United States. 3.1 Federal Communications Commission This device complies with part 15 of the Federal Communications Commission (FCC) Rules. Operation is subject to the following two conditions:

1. This device may not cause harmful interference 2. This device must accept any interference received, including interference that may cause undesired operation. NOTE: This equipment has been tested and found to comply with the limits for a Class B digital device, pursuant to Part 15 of the FCC Rules. These limits are designed to provide reasonable protection against harmful interference in a residential installation. This equipment generates uses and can radiate radio frequency energy and, if not installed and used in accordance with the instructions, may cause harmful interference to radio communications. However, there is no guarantee that interference will not occur in a particular installation. If this equipment does cause harmful interference to radio or television reception, which can be determined by turning the equipment off and on, the user is encouraged to try to correct the interference by one or more of the following measures:

Reorient or relocate the receiving antenna. Connect the equipment into an outlet on a circuit different from that to which the receiver is Increase the separation between the equipment and receiver. connected. Consult the dealer or an experienced radio/TV technician for help. Any changes or modifications not expressly approved by the manufacturer could void the users authority to operate the equipment. 4 GlowPack Function Description The GlowPack device works together with a Reminder Light device. The Reminder Light device is already certified by FCC (FCC ID: YOC373200). The GlowPack module is installed inside a Bag and used to store medicine that is pre-filled inside packs. This is the situation when the original GlowCap device cannot be used to store the medicine. It is potentially possible to contain other items inside the bag for general reminding function as long as the regular bag operation is not interfered. NantWorks Confidential and Proprietary Rev. 02 pg. 5 4.1 Hardware The GlowPack module is pre-installed inside the bag. As with GlowCaps, the medical dose time is pre-

programmed by doctors/nurses/medical specialists using the web interface to the Vitality servers. The Reminder Light will download this information from the servers, connecting via the cellular network. When it is time for a dose, the Reminder Light will pulse orange, and the LED in the GlowPack device will also pulse as an indicator. After a certain period is elapsed and if the dose has not been taken, the GlowPack will also play a quick sound pulse to remind the patient. Alternative reminding methods include placing a call to a and texting a message to the patients mobile phone. GlowPack module pre-installed NantWorks Confidential and Proprietary Rev. 02 pg. 6 LED glow at dose time Figure 2. GlowPack device and how it works with Vitality Reminder Light 4.2 Dose Time Configuration (For specialist only) The medication dose time may be change by doctors/nurses/medical specialists on the server. That information will go through the cellular network and be downloaded to the Reminder Light device paired with GlowPack device. A sample interface of this dose time setting is shown in the following graph. NantWorks Confidential and Proprietary Rev. 02 pg. 7 Figure 3. A sample server interface of how the medical dose time could be configured. For any questions and feedback, please send email to info@vitality.net or support@vitality.net NantWorks Confidential and Proprietary Rev. 02 pg. 8

		frequency	equipment class	purpose
1	2012-06-08	902 ~ 928	DXT - Part 15 Low Power Transceiver, Rx Verified	Original Equipment

Application Forms

app s	Applicant Information
1	Effective	2012-06-08
1	Applicant's complete, legal business name	NantWorks
1	FCC Registration Number (FRN)	0021679220
1	Physical Address	9920 Jefferson Blvd
1		Culver City, California 90232
1		United States

app s	TCB Information
1	TCB Application Email Address	t******@babt.com
1	TCB Scope	A1: Low Power Transmitters below 1 GHz (except Spread Spectrum), Unintentional Radiators, EAS (Part 11) & Consumer ISM devices

app s	FCC ID
1	Grantee Code	IFU
1	Equipment Product Code	380100

app s	Person at the applicant's address to receive grant or for contact
1	Name	D** L****
1	Title	Principal Engineer
1	Telephone Number	85836********
1	Fax Number	85836********
1	E-mail	d******@nantworks.com

app s	Technical Contact
		n/a

app s	Non Technical Contact
		n/a

app s	Confidentiality (long or short term)
1	Does this application include a request for confidentiality for any portion(s) of the data contained in this application pursuant to 47 CFR § 0.459 of the Commission Rules?:	Yes
1	Long-Term Confidentiality Does this application include a request for confidentiality for any portion(s) of the data contained in this application pursuant to 47 CFR § 0.459 of the Commission Rules?:	Yes
1	If so, specify the short-term confidentiality release date (MM/DD/YYYY format)	12/04/2012
	if no date is supplied, the release date will be set to 45 calendar days past the date of grant.

app s	Cognitive Radio & Software Defined Radio, Class, etc
1	Is this application for software defined/cognitive radio authorization?	No
1	Equipment Class	DXT - Part 15 Low Power Transceiver, Rx Verified
1	Description of product as it is marketed: (NOTE: This text will appear below the equipment class on the grant)	ISM 900 Vitality GlowPack
1	Related OET KnowledgeDataBase Inquiry: Is there a KDB inquiry associated with this application?	No
1	Modular Equipment Type	Does not apply
1	Purpose / Application is for	Original Equipment
1	Composite Equipment: Is the equipment in this application a composite device subject to an additional equipment authorization?	No
1	Related Equipment: Is the equipment in this application part of a system that operates with, or is marketed with, another device that requires an equipment authorization?	No
1	Is there an equipment authorization waiver associated with this application?	No
1	If there is an equipment authorization waiver associated with this application, has the associated waiver been approved and all information uploaded?	No

app s	Test Firm Name and Contact Information
1	Firm Name	TUV SUD America, Inc.
1	Name	C**** F**
1	Telephone Number	1-858********
1	Fax Number	1-858********
1	E-mail	c******@tuvam.com

Equipment Specifications
	Line	Rule Parts	Grant Notes	Lower Frequency	Upper Frequency	Power Output	Tolerance	Emission Designator	Microprocessor Number
1	1	15C		902.00000000	928.00000000

some individual PII (Personally Identifiable Information) available on the public forms may be redacted, original source may include additional details