510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K080455Substantially Equivalent

Rapidsense Drugs of Abuse Methamphetamine (Met) 1000 Device, Model 900-0050

Quantrx Biomedical Corporation, San Diego CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K080455 is the FDA 510(k) clearance record for RAPIDSENSE DRUGS OF ABUSE METHAMPHETAMINE (MET) 1000 DEVICE, MODEL 900-0050, a class II device, cleared for Quantrx Biomedical Corporation on under FDA product code LAF (Gas Chromatography, Methamphetamine). FDA records list 4 510(k) clearances for Quantrx Biomedical Corporation, from to . As of , FDA records show no recalls naming K080455.

Clearance record

Decision date
Received
(315 days to decision)
Product code
LAF Gas Chromatography, Methamphetamine
Regulation
21 CFR 862.3610
Device class
Class II
Review panel
Clinical Toxicology
Applicant
Quantrx Biomedical Corporation 13721 Via Tres Vista, San Diego CA
510(k) summary
Summary PDF
Third party review
No

Clearances, product code LAF

Trailing 12 months

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

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