Wondfo Methadone Urine Test (MTD 200), Wondofo Morphine Urine Test (Mop 100)

FDA 510(k) K131232 · Guangzhou Wondfo Biotech Co., Ltd.

Substantially Equivalent

510(k) numberK131232

Submission

Device name
Wondfo Methadone Urine Test (MTD 200), Wondofo Morphine Urine Test (Mop 100)
Applicant
Guangzhou Wondfo Biotech Co., Ltd.
Gaithersburg, MD, US
Received
May 1, 2013
Decision date
May 31, 2013
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
DJR – Enzyme Immunoassay, Methadone
Device class
Class II (moderate risk)
Regulation
21 CFR 862.3620
Specialty
Clinical Toxicology

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K170416LZI Methadone Metabolite Enzyme Immunoassay, LZI Methadone Metabolite (100 and 300)…DJR · Traditional Lin-Zhi International, Inc.06/26/2017SE
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K151441First Sign Drug of Abuse Dip Card Test, First Sign Drug of Abuse Cup TestDJR · Traditional W.H.P.M., Inc.06/29/2015SE
K092272Randox Methadone AssayDJR · Traditional Randox Laboratories, Ltd.11/18/2010SE
K092258Randox Metabolite (Eddp) AssayDJR · Traditional Randox Laboratories, Ltd.11/09/2010SE
K092048One Step Eddp (Methadone Metabolite) Test StripDJR · Traditional Biosite Incorporated04/19/2010SE

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Questions and answers

When was Wondfo Methadone Urine Test (MTD 200), Wondofo Morphine Urine Test (Mop 100) cleared by the FDA?

Wondfo Methadone Urine Test (MTD 200), Wondofo Morphine Urine Test (Mop 100) (K131232) received a 510(k) decision of Substantially Equivalent on May 31, 2013, 30 days after the submission was received.

What is the product code of K131232?

The FDA product code is DJR – Enzyme Immunoassay, Methadone, a Class II (moderate risk) device regulated under 21 CFR 862.3620.