510(k) K802755

ARTERIAL BLOOD FILTER BF-37 by Delta Medical Industries — Product Code DTM

K802755 is an FDA 510(k) premarket notification submitted by Delta Medical Industries for the device "ARTERIAL BLOOD FILTER BF-37". The FDA issued a decision of Substantially Equivalent on January 7, 1981. The device falls under product code DTM (Filter, Blood, Cardiopulmonary Bypass, Arterial Line), a Class II device regulated under 21 CFR 870.4260. Delta Medical Industries has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
January 7, 1981
Date Received
November 3, 1980
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