# K170973: VitalWatch Software User Interface

- Pathway: 510(k) (Traditional)
- Applicant: Vitalconnect, Inc.
- Decided: Jun 2, 2017 after 60 days
- Product code: DRG (Transmitters And Receivers, Physiological Signal, Radiofrequency)
- Device class: 2
- Regulation: 21 CFR 870.2910
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 9 generations back to K962603 (1997). 26 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 28 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K152139: Vital Connect Platform, HealthPatch MD, VitalPatch, Vitalconnect, Inc. (2015) Summary page 4.

## Most influential descendants
- K193343: Vista Solution Monitoring Kit, Vista Solution 2 10-day Evaluation Kit, VistaTablet 2 (Boxed) (2020), 0 descendants of its own

## Indications for use
VitalWatch is a software user interface intended for use by healthcare professionals to display physiological data collected by the VitalConnect Platform wireless remote monitoring system in home and healthcare settings. VitalWatch is a secondary, adjunct patient monitor and is not intended to replace existing standard-of-care patient monitoring practices.

Source page: https://510kreport.com/device/K170973
Methodology: https://510kreport.com/methodology