510(k) K900758

HEPARINIZED ARTERIAL SCREEN BLOOD FILTER by Cobe Laboratories, Inc. — Product Code DTM

K900758 is an FDA 510(k) premarket notification submitted by Cobe Laboratories, Inc. for the device "HEPARINIZED ARTERIAL SCREEN BLOOD FILTER". The FDA issued a decision of Substantially Equivalent on May 17, 1990. The device falls under product code DTM (Filter, Blood, Cardiopulmonary Bypass, Arterial Line), a Class II device regulated under 21 CFR 870.4260. Cobe Laboratories, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
May 17, 1990
Date Received
February 16, 1990
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Filter, Blood, Cardiopulmonary Bypass, Arterial Line
Device Class
Class II
Regulation Number
870.4260
Review Panel
CV
Submission Type