# Cardiomems, Inc.

- Location (FDA's records): Atlanta, GA
- FDA decisions: 5 (2005–2008): 4 510(k) clearances and 1 De Novo grant
- Product codes: NQH (5)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 0 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Recent decisions
- K082191: Cardiomems Endosure S2 Pressure Sensor with Delivery System, Model S2-2080 (Aug 19, 2008)
- K070680: Cardiomems Endosure S2 14F Wireless Aaa Pressure Measurement System, Model# S2-2080 (Apr 5, 2007)
- K070448: Cardiomems Endosure Wireless Aaa Pressure Measurement System, Model Ads-1001 (Mar 15, 2007)
- K061046: Cardiomems Endosure Pressure Sensor with Delivery System, Model Ads-1001 and Interrogator, Model Ems 5001 (Oct 12, 2006)
- DEN050006: Cardiomems Endosensor with Delivery System and Endosensor Electronics System (Oct 28, 2005)

Source page: https://510kreport.com/company/cardiomems