510(k) K955770

GAMMA GLUTAMYL TRANSFERASE TEST SYSTEM by Abaxis, Inc. — Product Code JQB

K955770 is an FDA 510(k) premarket notification submitted by Abaxis, Inc. for the device "GAMMA GLUTAMYL TRANSFERASE TEST SYSTEM". The FDA issued a decision of Substantially Equivalent on September 9, 1996. The device falls under product code JQB (Kinetic Method, Gamma-Glutamyl Transpeptidase), a Class I device regulated under 21 CFR 862.1360. Abaxis, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
September 9, 1996
Date Received
December 21, 1995
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Kinetic Method, Gamma-Glutamyl Transpeptidase
Device Class
Class I
Regulation Number
862.1360
Review Panel
CH
Submission Type