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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