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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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