Medical Device
Manufacturing
THE TRADE PAPER OF THE FACTORY FLOOR
K925337Substantially Equivalent

Olympus Gamma Glutamyl Transferase Reagent

Olympus Corp., Lake Success NY / Traditional, Substantially Equivalent

K925337 is the FDA 510(k) clearance record for OLYMPUS GAMMA GLUTAMYL TRANSFERASE REAGENT, a class I device, cleared for Olympus Corp. on under FDA product code JQB (Kinetic Method, Gamma-Glutamyl Transpeptidase). FDA records list 149 510(k) clearances for Olympus Corp., from to . As of , FDA records show no recalls naming K925337.

Clearance record

Decision date
Received
(98 days to decision)
Product code
JQB Kinetic Method, Gamma-Glutamyl Transpeptidase
Regulation
21 CFR 862.1360
Device class
Class I
Review panel
Clinical Chemistry
Applicant
Olympus Corp. 4 Nevada Dr., Lake Success NY
510(k) summary
Statement
Third party review
No

Clearances, product code JQB

Trailing 12 months

FDA records hold no clearances under product code JQB in the trailing twelve months.

FDA records show no clearances under product code JQB in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code JQB, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260