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FDA 510(k) Applications Submitted by DATASCOPE CORP., CARDIAC ASSIST DIVISION
FDA 510(k) Number
Submission Date
Device Name
Applicant
K122405
08/07/2012
AIR-BAND RADIAL COMPRESSION DEVICE
DATASCOPE CORP., CARDIAC ASSIST DIVISION
K122628
08/28/2012
SENSATION PLUS 7.5FR. 40CC INTRA-AORTIC BALLOON (IAB) CATHETER AND ACCESSORIES
DATASCOPE CORP., CARDIAC ASSIST DIVISION
K091449
05/18/2009
DATASCOPE'S 8FR. 50CC INTRA-AORTIC BALLOON CATHETER AND ACCESSORIES, MODELS 0684,00-0498-01, 02
DATASCOPE CORP., CARDIAC ASSIST DIVISION
K120868
03/22/2012
MEGA(TM) 7.5FR. 30CC INTRA-AORTIC BALLOON CATHETER AND ACCESSORIES, MEGA(TM) 7.5FR. 40CC INTRA-AORTIC BALLOON CATHETER
DATASCOPE CORP., CARDIAC ASSIST DIVISION
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