510(k) K030077

GISH TUBING AND CONNECTORS WITH GBS COATING by Gish Biomedical, Inc. — Product Code DTL

K030077 is an FDA 510(k) premarket notification submitted by Gish Biomedical, Inc. for the device "GISH TUBING AND CONNECTORS WITH GBS COATING". The FDA issued a decision of Substantially Equivalent on March 14, 2003. The device falls under product code DTL (Adaptor, Stopcock, Manifold, Fitting, Cardiopulmonary Bypass), a Class II device regulated under 21 CFR 870.4290. Gish Biomedical, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
March 14, 2003
Date Received
January 8, 2003
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Adaptor, Stopcock, Manifold, Fitting, Cardiopulmonary Bypass
Device Class
Class II
Regulation Number
870.4290
Review Panel
CV
Submission Type