510(k) K925337

OLYMPUS GAMMA GLUTAMYL TRANSFERASE REAGENT by Olympus Corp. — Product Code JQB

K925337 is an FDA 510(k) premarket notification submitted by Olympus Corp. for the device "OLYMPUS GAMMA GLUTAMYL TRANSFERASE REAGENT". The FDA issued a decision of Substantially Equivalent on January 26, 1993. The device falls under product code JQB (Kinetic Method, Gamma-Glutamyl Transpeptidase), a Class I device regulated under 21 CFR 862.1360. Olympus Corp. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
January 26, 1993
Date Received
October 20, 1992
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