510(k) K952532

AFFINITY ARTERIAL BLOOD FILTER by Avecor Cardiovascular, Inc. — Product Code DTM

K952532 is an FDA 510(k) premarket notification submitted by Avecor Cardiovascular, Inc. for the device "AFFINITY ARTERIAL BLOOD FILTER". The FDA issued a decision of Substantially Equivalent on October 6, 1995. The device falls under product code DTM (Filter, Blood, Cardiopulmonary Bypass, Arterial Line), a Class II device regulated under 21 CFR 870.4260. Avecor Cardiovascular, Inc. has at least 8 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
October 6, 1995
Date Received
June 1, 1995
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