# Cardiva Medical, Inc.

- Location (FDA's records): Sunnyvale, CA
- FDA decisions: 9 (2004–2013): 7 510(k) clearances and 2 original PMA approvals
- Product codes: DXC (7), MGB (2)
- Predicates its devices cite: 12 (8 its own); citations of its devices by later devices: 10 (8 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
- Radi Medical Systems AB: 2 (https://510kreport.com/company/radi-medical-systems)
- Cardiothoracic Systems, Inc.: 2 (https://510kreport.com/company/cardiothoracic-systems)

## Firms that cite its devices most
- Arstasis, Inc.: 2 (https://510kreport.com/company/arstasis)

## Its most-cited devices
- K041486: Vasostasis Vascular Closure System (2004), cited by 3
- K070485: Boomerang Wire /Boomerang Plus Wire System, Model# B Plus Wire 58L (2007), cited by 2
- K072297: Boomerang Catalyst/Boomerang Catalyst II System (2007), cited by 2
- K051817: Boomerang Closurewire Vascular Closure System (2006), cited by 1
- K061075: Boomerang Wire (2006), cited by 1
- K082930: Cardiva Catalyst Iii System with Protamine Sulfate (2009), cited by 1

## Recent decisions
- K130124: Catalyst II and Iii (Mar 14, 2013)
- P120016: Vascade Vascular Closure System (Jan 31, 2013)
- P080029: Quick-Close Vascular Suturing System (Quick-Close System) (Apr 8, 2010)
- K082930: Cardiva Catalyst Iii System with Protamine Sulfate (Feb 13, 2009)
- K072297: Boomerang Catalyst/Boomerang Catalyst II System (Sep 12, 2007)
- K070485: Boomerang Wire /Boomerang Plus Wire System, Model# B Plus Wire 58L (Mar 22, 2007)
- K051817: Boomerang Closurewire Vascular Closure System (Dec 6, 2006)
- K061075: Boomerang Wire (Sep 1, 2006)

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