# K090610: Hospira Vital Signs Wireless Monitoring System

- Pathway: 510(k) (Traditional)
- Applicant: Hospira, Inc.
- Decided: Mar 13, 2009 after 7 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: 3 generations back to K891104 (1989). 5 ancestors in all.
9 later devices descend from it; 3 cite it directly.
0 of 15 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K053016: Wireless Physiologic Monitoring System, Edwards Lifesciences, LLC (2005) Summary page 1.
- K030795: Lifesyne Systems, Gmp/Companies, Inc. (2003) Summary page 1.

## Most influential descendants
- K142476: Master Caution Device MCD (2015), 6 descendants of its own
- K161431: SimplECG (2016), 5 descendants of its own
- K201669: SimpleSENSE (2020), 3 descendants of its own
- K212160: SimpleSENSE Platform (2021), 1 descendant of its own
- K243981: Hexoskin Medical System (7100-00016) (2025), 0 descendants of its own

## Indications for use
Hospira Vital Signs Wireless Monitoring System is indicated for use on patients requiring pressure monitoring. Hospira Vital Signs Wireless Monitoring System is intended to perform wireless transmission of pressure information to remote patient monitors from disposable pressure transducers.

Source page: https://510kreport.com/device/K090610
Methodology: https://510kreport.com/methodology