510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K932209Substantially Equivalent

Toxi*lab Ltd Opiate System

Toxi-Lab, Inc., Irvine CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K932209 is the FDA 510(k) clearance record for TOXI*LAB LTD OPIATE SYSTEM, a class II device, cleared for Toxi-Lab, Inc. on under FDA product code LAI (Thin Layer Chromatography, Opiates). FDA records list 5 510(k) clearances for Toxi-Lab, Inc., from to . As of , FDA records show no recalls naming K932209.

Clearance record

Decision date
Received
(141 days to decision)
Product code
LAI Thin Layer Chromatography, Opiates
Regulation
21 CFR 862.3650
Device class
Class II
Review panel
Clinical Toxicology
Applicant
Toxi-Lab, Inc. 2 Goodyear, Irvine CA
510(k) summary
Summary
Third party review
No

Clearances, product code LAI

Trailing 12 months

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

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