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) cleared devices by 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