FDA 510(k), K063723, IMPELLA RECOVER LP 2.5 PERCUTANEOUS CARDIAC SUPPORT SYSTEM
FDA 510(k), K063723, IMPELLA RECOVER LP 2.5 PERCUTANEOUS CARDIAC SUPPORT SYSTEM
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$149.00 USD
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510(K) Number: K063723
Device Name: IMPELLA RECOVER LP 2.5 PERCUTANEOUS CARDIAC SUPPORT SYSTEM
Manufacturer:
Device Classification Name: Pump, Blood, Cardiopulmonary Bypass, Non-Roller Type
Regulation Number: 870.4360
Classification Product Code: KFM
Date Received: 12/15/2006
Decision Date: 05/30/2008
Regulation Medical Specialty: Cardiovascular
Device Name: IMPELLA RECOVER LP 2.5 PERCUTANEOUS CARDIAC SUPPORT SYSTEM
Manufacturer:
Device Classification Name: Pump, Blood, Cardiopulmonary Bypass, Non-Roller Type
Regulation Number: 870.4360
Classification Product Code: KFM
Date Received: 12/15/2006
Decision Date: 05/30/2008
Regulation Medical Specialty: Cardiovascular