FDA 510(k) Applications Submitted by POLYSTAN A/S

FDA 510(k) Number Submission Date Device Name Applicant
K022281 07/15/2002 SAFE MAXI VENOUS/CARDIOTOMY RESERVIOR, MODEL 016045 POLYSTAN A/S
K013038 09/10/2001 SAFE MAXI HOLLOW FIBER OXYGENATOR, MODEL 016010 POLYSTAN A/S
K023251 09/30/2002 PEDIATRIC ARTERIAL CANNULA POLYSTAN A/S
K953976 08/23/1995 SAFE MICRO POLYSTAN A/S
K980974 03/16/1998 SAFE MINI POLYSTAN A/S


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