Rapidone - Marijuana Test

FDA 510(k) K990818 · American Bio Medica Corp.

Substantially Equivalent

510(k) numberK990818

Submission

Device name
Rapidone - Marijuana Test
Applicant
American Bio Medica Corp.
Washington, DC, US
Received
March 11, 1999
Decision date
July 7, 1999
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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K041712'Rapidtec 4' TestDIS · Traditional 11/03/2004SE
K030835'Rapid One' - Propoxyphene TestJXN · Traditional 05/22/2003SE
K023869'RAPIDTEC'-5M-MULTIPLE Dip TestDJR · Traditional 04/30/2003SE
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Questions and answers

When was Rapidone - Marijuana Test cleared by the FDA?

Rapidone - Marijuana Test (K990818) received a 510(k) decision of Substantially Equivalent on July 7, 1999, 118 days after the submission was received.

What is the product code of K990818?

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