Cardiva Medical, Inc. is one of 5253 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Cardiva Medical, Inc. - FDA 510(k) Cleared Devices
7
Total
7
Cleared
0
Denied
Cardiva Medical, Inc. has 7 FDA 510(k) cleared medical devices. Based in Pleasanton, US.
Historical record: 7 cleared submissions from 2004 to 2013. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Cardiva Medical, Inc. Filter by specialty or product code using the sidebar.
Cardiva Medical, Inc. — FDA 510(k) Products and Clearance History
7 devices
Cleared
Mar 14, 2013
CATALYST II AND III
Cardiovascular
56d
Cleared
Feb 13, 2009
CARDIVA CATALYST III SYSTEM WITH PROTAMINE SULFATE
Cardiovascular
135d
Cleared
Sep 12, 2007
BOOMERANG CATALYST/BOOMERANG CATALYST II SYSTEM
Cardiovascular
26d
Cleared
Mar 22, 2007
BOOMERANG WIRE /BOOMERANG PLUS WIRE SYSTEM, MODEL# B PLUS WIRE 58L
Cardiovascular
30d
Cleared
Dec 06, 2006
BOOMERANG CLOSUREWIRE VASCULAR CLOSURE SYSTEM
Cardiovascular
519d
Cleared
Sep 01, 2006
BOOMERANG WIRE
Cardiovascular
137d
Cleared
Oct 22, 2004
VASOSTASIS VASCULAR CLOSURE SYSTEM
Cardiovascular
140d