Cardiva Medical, Inc.
FDA 510(k) & PMA Approved Devices — 7 products
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Total Devices7
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K130124 | CATALYST II AND III | DXC | 2013-03-14 | View |
| 510(k) | K082930 | CARDIVA CATALYST III SYSTEM WITH PROTAMINE SULFATE | DXC | 2009-02-13 | View |
| 510(k) | K072297 | BOOMERANG CATALYST/BOOMERANG CATALYST II SYSTEM | DXC | 2007-09-12 | View |
| 510(k) | K070485 | BOOMERANG WIRE /BOOMERANG PLUS WIRE SYSTEM, MODEL# B PLUS WIRE 58L | DXC | 2007-03-22 | View |
| 510(k) | K051817 | BOOMERANG CLOSUREWIRE VASCULAR CLOSURE SYSTEM | DXC | 2006-12-06 | View |
| 510(k) | K061075 | BOOMERANG WIRE | DXC | 2006-09-01 | View |
| 510(k) | K041486 | VASOSTASIS VASCULAR CLOSURE SYSTEM | DXC | 2004-10-22 | View |
No matching devices.
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