Medical Device
Manufacturing
THE TRADE PAPER OF THE FACTORY FLOOR
K903223Substantially Equivalent

On-Site Alcohol

Toxi-Lab, Inc., Irvine CA / Traditional, Substantially Equivalent

K903223 is the FDA 510(k) clearance record for ON-SITE ALCOHOL, a class II device, cleared for Toxi-Lab, Inc. on under FDA product code DOJ (Potassium Dichromate, Alcohol). FDA records list 5 510(k) clearances for Toxi-Lab, Inc., from to . As of , FDA records show no recalls naming K903223.

Clearance record

Decision date
Received
(233 days to decision)
Product code
DOJ Potassium Dichromate, Alcohol
Regulation
21 CFR 862.3040
Device class
Class II
Review panel
Clinical Toxicology
Applicant
Toxi-Lab, Inc. 2 Goodyear, Irvine CA
Third party review
No

Clearances, product code DOJ

Trailing 12 months

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

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