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

FDA 510(k) K080455 · Quantrx Biomedical Corporation

Substantially Equivalent

510(k) numberK080455

Submission

Device name
Rapidsense Drugs of Abuse Methamphetamine (Met) 1000 Device, Model 900-0050
Applicant
Quantrx Biomedical Corporation
San Diego, CA, US
Received
February 20, 2008
Decision date
December 31, 2008
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
LAF – Gas Chromatography, Methamphetamine
Device class
Class II (moderate risk)
Regulation
21 CFR 862.3610
Specialty
Clinical Toxicology

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More from Lin-Zhi International, Inc.

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Questions and answers

When was Rapidsense Drugs of Abuse Methamphetamine (Met) 1000 Device, Model 900-0050 cleared by the FDA?

Rapidsense Drugs of Abuse Methamphetamine (Met) 1000 Device, Model 900-0050 (K080455) received a 510(k) decision of Substantially Equivalent on December 31, 2008, 315 days after the submission was received.

What is the product code of K080455?

The FDA product code is LAF – Gas Chromatography, Methamphetamine, a Class II (moderate risk) device regulated under 21 CFR 862.3610.