Medical Device
Manufacturing
THE TRADE PAPER OF THE FACTORY FLOOR
K931939Substantially Equivalent

Olympus Creatinine Reagent

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

K931939 is the FDA 510(k) clearance record for OLYMPUS CREATININE REAGENT, a class II device, cleared for Olympus Corp. on under FDA product code CGX (Alkaline Picrate, Colorimetry, Creatinine). FDA records list 149 510(k) clearances for Olympus Corp., from to . As of , FDA records show no recalls naming K931939.

Clearance record

Decision date
Received
(155 days to decision)
Product code
CGX Alkaline Picrate, Colorimetry, Creatinine
Regulation
21 CFR 862.1225
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 CGX

Trailing 12 months
2 clearances under product code CGX in the twelve months to October 2026, November 2025 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code CGX, trailing twelve months
MonthClearances
November 20251
December 20250
January 20261
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260