# K130957: WVSM (Wirless Vital Signs Monitor)

- Pathway: 510(k) (Special)
- Applicant: Athena Gtx
- Decided: Apr 30, 2013 after 25 days
- Product code: MWI (Monitor, Physiological, Patient (Without Arrhythmia Detection Or Alarms))
- Device class: 2
- Regulation: 21 CFR 870.2300
- 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). 31 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 33 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K101674: WVSM (Wireless Vital Signs Monitor), Model 5.0, Athena Gtx (2010)

## Most influential descendants
- K173203: Athena GTX Device Management Suite (ADMS) Software (2018), 0 descendants of its own

## Indications for use
The Wireless Vital Signs Monitor (WVSM) is intended to be used as an adult patient monitor. It is indicated as a single or multi-parameter vital signs monitor for ECG, noninvasive blood pressure (NIBP) and SpO2. It may be used in the following locations: Hospitals, healthcare facilities, emergency medical applications, during transport, and other healthcare applications. The monitor uses wireless communications to transmit vital signs data to a handheld or PC computer. The monitor is intended to be used by trained healthcare providers.

Source page: https://510kreport.com/device/K130957
Methodology: https://510kreport.com/methodology