Medical Device
Manufacturing
THE TRADE PAPER OF THE FACTORY FLOOR
K924832Substantially Equivalent

Olympus Creatine Kinase Reagent

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

K924832 is the FDA 510(k) clearance record for OLYMPUS CREATINE KINASE REAGENT, a class II device, cleared for Olympus Corp. on under FDA product code CGS (Nad Reduction/Nadh Oxidation, Cpk Or Isoenzymes). FDA records list 149 510(k) clearances for Olympus Corp., from to . As of , FDA records show no recalls naming K924832.

Clearance record

Decision date
Received
(101 days to decision)
Product code
CGS Nad Reduction/Nadh Oxidation, Cpk Or Isoenzymes
Regulation
21 CFR 862.1215
Device class
Class II
Review panel
Clinical Chemistry
Applicant
Olympus Corp. 4 Nevada Dr., Lake Success NY
510(k) summary
Statement
Third party review
No

Clearances, product code CGS

Trailing 12 months

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

FDA records show no clearances under product code CGS in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code CGS, 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