510(k) K922230

OLYMPUS GGT REAGENT by Olympus Corp. — Product Code JQB

K922230 is an FDA 510(k) premarket notification submitted by Olympus Corp. for the device "OLYMPUS GGT REAGENT". The FDA issued a decision of Substantially Equivalent on June 25, 1992. 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
June 25, 1992
Date Received
May 12, 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