# Appriva Medical, Inc.

- Location (FDA's records): Sunnyvale, CA
- FDA decisions: 2 (2001–2001): 2 510(k) clearances
- Product codes: DYB (2)
- Predicates its devices cite: 1 (1 its own); citations of its devices by later devices: 3 (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 that cite its devices most
- Velocimed, Inc.: 1 (https://510kreport.com/company/velocimed)
- Evalve, Inc.: 1 (https://510kreport.com/company/evalve)

## Its most-cited devices
- K002054: X-Sept Transseptal Sheath and Transition Catheter, Model MV-03-09-90, MV-03-10-90, MV-03-11-90, MV-03-09-120, MV-03-10-1 (2001), cited by 2
- K012489: Modification to: X-Sept Transseptal Shealth and Transition Catheter (with Dilator), Models PL-12-12-09, PL-12-12-10 (2001), cited by 1

## Recent decisions
- K012489: Modification to: X-Sept Transseptal Shealth and Transition Catheter (with Dilator), Models PL-12-12-09, PL-12-12-10 (Aug 30, 2001)
- K002054: X-Sept Transseptal Sheath and Transition Catheter, Model MV-03-09-90, MV-03-10-90, MV-03-11-90, MV-03-09-120, MV-03-10-1 (Feb 16, 2001)

Source page: https://510kreport.com/company/appriva-medical