FDA 510(k) Applications for Medical Device Product Code: KRJ (Filter, Prebypass, Cardiopulmonary Bypass)

FDA 510(k) Applications for Medical Device Product Code "KRJ"
(Filter, Prebypass, Cardiopulmonary Bypass)

FDA 510(k) Number	Applicant	Device Name	Decision Date
K982385	POROUS MEDIA CORP.	POROUS MEDIA DPB20 SERIES DISPOSABLE PRE-BYPASS FILTER	02/01/1999
K990276	POROUS MEDIA CORP.	POROUS MEDIA DPB30 SERIES DISPOSABLE PRE-BYPASS FILTER	10/01/1999