Cardiva Medical, Inc.
Cardiva Medical, Inc. holds FDA 510(k) medical device clearances, first cleared 2004, most recent 2013.
Top product codes for Cardiva Medical, Inc.
Recent clearances by Cardiva Medical, Inc.
- K130124 — CATALYST II AND III
- K082930 — CARDIVA CATALYST III SYSTEM WITH PROTAMINE SULFATE
- K072297 — BOOMERANG CATALYST/BOOMERANG CATALYST II SYSTEM
- K070485 — BOOMERANG WIRE /BOOMERANG PLUS WIRE SYSTEM, MODEL# B PLUS WIRE 58L
- K051817 — BOOMERANG CLOSUREWIRE VASCULAR CLOSURE SYSTEM
- K061075 — BOOMERANG WIRE
- K041486 — VASOSTASIS VASCULAR CLOSURE SYSTEM
Data sourced from openFDA. This site is unofficial and independent of the FDA.