Amedica Drug Screen THC Test

FDA 510(k) K022955 · Amedica Biotech, Inc.

Substantially Equivalent

510(k) numberK022955

Submission

Device name
Amedica Drug Screen THC Test
Applicant
Amedica Biotech, Inc.
Hayward, CA, US
Received
September 5, 2002
Decision date
November 6, 2002
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
LDJ – Enzyme Immunoassay, Cannabinoids
Device class
Class II (moderate risk)
Regulation
21 CFR 862.3870
Specialty
Clinical Toxicology

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More from Healgen Scientific,, LLC

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K031497Amedica Drug Screen Mdma-Bar-Bzo-Mtd-Tca TestDJC · Traditional 10/17/2003SE
K023109Amedica Drug Screen Phencyclidine TestLCM · Traditional 12/16/2002SE
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Questions and answers

When was Amedica Drug Screen THC Test cleared by the FDA?

Amedica Drug Screen THC Test (K022955) received a 510(k) decision of Substantially Equivalent on November 6, 2002, 62 days after the submission was received.

What is the product code of K022955?

The FDA product code is LDJ – Enzyme Immunoassay, Cannabinoids, a Class II (moderate risk) device regulated under 21 CFR 862.3870.