FDA 510(k) Applications Submitted by CARDIVA MEDICAL, INC.

FDA 510(k) Number Submission Date Device Name Applicant
K041486 06/04/2004 VASOSTASIS VASCULAR CLOSURE SYSTEM CARDIVA MEDICAL, INC.
K061075 04/17/2006 BOOMERANG WIRE CARDIVA MEDICAL, INC.
K051817 07/05/2005 BOOMERANG CLOSUREWIRE VASCULAR CLOSURE SYSTEM CARDIVA MEDICAL, INC.
K072297 08/17/2007 BOOMERANG CATALYST/BOOMERANG CATALYST II SYSTEM CARDIVA MEDICAL, INC.
K082930 10/01/2008 CARDIVA CATALYST III SYSTEM WITH PROTAMINE SULFATE CARDIVA MEDICAL, INC.
K130124 01/17/2013 CATALYST II AND III CARDIVA MEDICAL, INC.
K070485 02/20/2007 BOOMERANG WIRE /BOOMERANG PLUS WIRE SYSTEM, MODEL# B PLUS WIRE 58L CARDIVA MEDICAL, INC.


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