# K173203: Athena GTX Device Management Suite (ADMS) Software

- Pathway: 510(k) (Traditional)
- Applicant: Athena Gtx
- Decided: Mar 14, 2018 after 163 days
- Product code: MSX (System, Network And Communication, Physiological Monitors)
- 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: 26 generations back to K941811 (1994). 165 ancestors in all.
No later device cites it as a predicate yet.
0 of 166 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K163584: M3290B Philips IntelliVue Information Center iX, Philips Medical Systems (2017) Summary page 4.
- K130957: WVSM (Wirless Vital Signs Monitor), Athena Gtx (2013) Summary page 4.

## Indications for use
The intended use of the ADMS software application is to: Receive, aggregate, process, distribute and display physiologic waves, parameters, alarms and events at locations other than at the patient, for multiple patients. Display visual alarm conditions as generated by a connected monitor. Display of patient information can be real-time or historical record review. Provide review and trend application data, designed to contribute to the screening of patient condition. All information or visual indications provided are intended to support the judgement of a medical professional and are not intended to be the sole source of information for decision making. Provide connection to other systems not associated with active patient monitoring, such as information systems. The software performs the action to transfer, store, convert from one format to another according to preset specifications, or to display medical device data. ADMS is intended for use in professional healthcare facilities, emergency medical applications, during transport, and other healthcare environments by trained healthcare professionals. ADMS Software is not intended for home use. Indicated for use for specific patient populations (adult, pediatric, infant/neonate) depends on the indicated labeling of medical device(s) connected to ADMS providing the data.

Source page: https://510kreport.com/device/K173203
Methodology: https://510kreport.com/methodology