510(k) K820679

PEDIATRIC ARTERIAL BLOOD FILTER #AF-540 by Bentley Laboratories, Inc. — Product Code DTM

K820679 is an FDA 510(k) premarket notification submitted by Bentley Laboratories, Inc. for the device "PEDIATRIC ARTERIAL BLOOD FILTER #AF-540". The FDA issued a decision of Substantially Equivalent on June 17, 1982. The device falls under product code DTM (Filter, Blood, Cardiopulmonary Bypass, Arterial Line), a Class II device regulated under 21 CFR 870.4260. Bentley Laboratories, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
June 17, 1982
Date Received
March 11, 1982
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