510(k) K023833

GISH ARTERIAL FILTER WITH GBS COATING by Gish Biomedical, Inc. — Product Code DTM

K023833 is an FDA 510(k) premarket notification submitted by Gish Biomedical, Inc. for the device "GISH ARTERIAL FILTER WITH GBS COATING". The FDA issued a decision of Substantially Equivalent on March 31, 2003. The device falls under product code DTM (Filter, Blood, Cardiopulmonary Bypass, Arterial Line), a Class II device regulated under 21 CFR 870.4260. Gish Biomedical, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
March 31, 2003
Date Received
November 18, 2002
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