Company ยท US
Cardiva Medical, Inc.
FDA 510(k) clearances and medical device recalls filed under this name, 2004 to 2013. Name variants (Inc, Corp, punctuation) are merged.
7510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)
Product codes
| Code | Device | Records |
|---|---|---|
| DXC | Clamp, Vascular | 7 |
Latest 510(k) clearances
| Decided | 510(k) | Device and applicant | Code |
|---|---|---|---|
| Mar 14, 2013 | K130124 | CATALYST II AND III Cardiva Medical, Inc. | DXC |
| Feb 13, 2009 | K082930 | CARDIVA CATALYST III SYSTEM WITH PROTAMINE SULFATE Cardiva Medical, Inc. | DXC |
| Sep 12, 2007 | K072297 | BOOMERANG CATALYST/BOOMERANG CATALYST II SYSTEM Cardiva Medical, Inc. | DXC |
| Mar 22, 2007 | K070485 | BOOMERANG WIRE /BOOMERANG PLUS WIRE SYSTEM, MODEL# B PLUS WIRE 58L Cardiva Medical, Inc. | DXC |
| Dec 6, 2006 | K051817 | BOOMERANG CLOSUREWIRE VASCULAR CLOSURE SYSTEM Cardiva Medical, Inc. | DXC |
| Sep 1, 2006 | K061075 | BOOMERANG WIRE Cardiva Medical, Inc. | DXC |
| Oct 22, 2004 | K041486 | VASOSTASIS VASCULAR CLOSURE SYSTEM Cardiva Medical, Inc. | DXC |
Latest recalls
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| No recalls in this window. | |||