Datascope Corp., Cardiac Assist Division is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Datascope Corp., Cardiac Assist Division - FDA 510(k) Cleared Devices
4
Total
4
Cleared
0
Denied
Datascope Corp., Cardiac Assist Division has 4 FDA 510(k) cleared medical devices. Based in Fairfield, US.
Historical record: 4 cleared submissions from 2009 to 2012. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Datascope Corp., Cardiac Assist Division Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Datascope Corp., Cardiac Assist Division
4 devices
Cleared
Nov 09, 2012
AIR-BAND RADIAL COMPRESSION DEVICE
Cardiovascular
94d
Cleared
Sep 06, 2012
SENSATION PLUS 7.5FR. 40CC INTRA-AORTIC BALLOON (IAB) CATHETER AND ACCESSORIES
Cardiovascular
9d
Cleared
Apr 20, 2012
MEGA(TM) 7.5FR. 30CC INTRA-AORTIC BALLOON CATHETER AND ACCESSORIES, MEGA(TM)...
Cardiovascular
29d
Cleared
Jun 18, 2009
DATASCOPE'S 8FR. 50CC INTRA-AORTIC BALLOON CATHETER AND ACCESSORIES, MODELS...
Cardiovascular
31d