FDA 510(k) Application Details - K001787

Device Classification Name	Filter, Blood, Cardiopulmonary Bypass, Arterial Line   More FDA Info for this Device
510(K) Number	K001787
Device Name	Filter, Blood, Cardiopulmonary Bypass, Arterial Line
Applicant	JOSTRA MEDIZINTECHNIK AG 2035 SUNSET LAKE RD. NEWARK, DE 19702 US Other 510(k) Applications for this Company
Contact	KATHY JOHNSON Other 510(k) Applications for this Contact
Regulation Number	870.4260   More FDA Info for this Regulation Number
Classification Product Code	DTM Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	06/13/2000
Decision Date	06/30/2000
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	CV - Cardiovascular
Review Advisory Committee	CV - Cardiovascular
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review