# Mespere Lifesciences, Inc.

- Location (FDA's records): Waterloo, CA
- FDA decisions: 3 (2013–2018): 3 510(k) clearances
- Product codes: PFA (2), QEM (1)
- Predicates its devices cite: 5 (1 its own); citations of its devices by later devices: 1 (1 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Edwards Lifesciences, LLC: 1 (https://510kreport.com/company/edwards-lifesciences)
- Covidien: 1 (https://510kreport.com/company/covidien)
- Draeger Medical Systems, Inc.: 1 (https://510kreport.com/company/draeger-medical-systems)
- Somanetics Corp.: 1 (https://510kreport.com/company/somanetics)

## Its most-cited devices
- K131085: Central Venous Pressure System - Mespere Venus 1000 (2013), cited by 1

## Recent decisions
- K182242: VO200 – NeurOs Cerebral Oximetry System (Dec 26, 2018)
- K151776: Central Venous Pressure System (Aug 12, 2015)
- K131085: Central Venous Pressure System - Mespere Venus 1000 (Aug 22, 2013)

Source page: https://510kreport.com/company/mespere-lifesciences