# K132447: Vitalconnect Platform by Vital Connect Inc.

- Pathway: 510(k) (Traditional)
- Applicant: Vitalconnect, Inc.
- Decided: Apr 3, 2014 after 240 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: 20 generations back to K941811 (1994). 129 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 131 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K110809: Wireless Monitoring System, Carefusion 303, Inc. (2011) Summary page 1.
- K121197: Bodyguardian System Bodyguardian Control Unit Bodyguardian Connect, Preventice, Inc. (2012) Summary page 1.
- K083287: Avivo Mobile Patient Management System, Corventis, Inc. (2009) Summary page 1.

## Most influential descendants
- K191870: VV330 Continuous ECG Platform, VivaLNK Adhesive Patch (2020), 0 descendants of its own

## Indications for use
The VitalConnect Platform is a wireless monitoring system intended for use by healthcare professionals for unattended surveillance of physiological data within healthcare settings. This includes heart rate, electrocardiography (ECG), heart rate variability, respiratory rate, skin temperature, activity (including step count), and posture (body position relative to gravity including fall). Data is transmitted wirelessly to a central location where it is stored for analysis. The VitalConnect Platform can be configured by Authorized Persons to notify healthcare professionals when physiological data falls outside selected parameters. The device is not intended to be used on critical care patients and is intended to supplement vital signs monitoring by healthcare professionals, not to replace current standards of care. The device is intended for use on general care patients and on patients who are 18 years of age or older. It is not intended for home use.

Source page: https://510kreport.com/device/K132447
Methodology: https://510kreport.com/methodology