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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name system, balloon, intra-aortic and control
510(k) Number K122628
Device Name SENSATION PLUS 7.5FR. 40CC INTRA-AORTIC BALLOON (IAB) CATHETER AND ACCESSORIES
Applicant
DATASCOPE CORP., CARDIAC ASSIST DIVISION
15 LAW DR.
FAIRFIELD,  NJ  07004 -0011
Applicant Contact CARLA S CERQUEIRA
Correspondent
DATASCOPE CORP., CARDIAC ASSIST DIVISION
15 LAW DR.
FAIRFIELD,  NJ  07004 -0011
Correspondent Contact CARLA S CERQUEIRA
Regulation Number870.3535
Classification Product Code
DSP  
Date Received08/28/2012
Decision Date 09/06/2012
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Cardiovascular
510k Review Panel Cardiovascular
Summary Summary
Type Special
Reviewed by Third Party No
Combination Product No
Recalls CDRH Recalls
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