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FDA 510(k), K982385, POROUS MEDIA DPB20 SERIES DISPOSABLE PRE-BYPASS FILTER
FDA 510(k), K982385, POROUS MEDIA DPB20 SERIES DISPOSABLE PRE-BYPASS FILTER
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$149.00 USD
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$149.00 USD
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510(K) Number: K982385
Device Name: POROUS MEDIA DPB20 SERIES DISPOSABLE PRE-BYPASS FILTER
Manufacturer:
Device Classification Name: Filter, Prebypass, Cardiopulmonary Bypass
Regulation Number: 870.4280
Classification Product Code: KRJ
Date Received: 07/09/1998
Decision Date: 02/01/1999
Regulation Medical Specialty: Cardiovascular
Device Name: POROUS MEDIA DPB20 SERIES DISPOSABLE PRE-BYPASS FILTER
Manufacturer:
Device Classification Name: Filter, Prebypass, Cardiopulmonary Bypass
Regulation Number: 870.4280
Classification Product Code: KRJ
Date Received: 07/09/1998
Decision Date: 02/01/1999
Regulation Medical Specialty: Cardiovascular
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