Medical Device
Manufacturing
THE TRADE PAPER OF THE FACTORY FLOOR
K902572Substantially Equivalent

Sodium Reagent Set

Tech Intl. Co., Rochester Hills MI / Traditional, Substantially Equivalent

K902572 is the FDA 510(k) clearance record for SODIUM REAGENT SET, a class II device, cleared for Tech Intl. Co. on under FDA product code CEI (Uranyl Acetate/Zinc Acetate, Sodium). FDA records list 13 510(k) clearances for Tech Intl. Co., from to . As of , FDA records show no recalls naming K902572.

Clearance record

Decision date
Received
(29 days to decision)
Product code
CEI Uranyl Acetate/Zinc Acetate, Sodium
Regulation
21 CFR 862.1665
Device class
Class II
Review panel
Clinical Chemistry
Applicant
Tech Intl. Co. 1856 Starr-Batt Dr., Rochester Hills MI
Third party review
No

Clearances, product code CEI

Trailing 12 months

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

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