Screeners Marijuana Test, Drugscreen Dip Marijuana Test

FDA 510(k) K992949 · Drug Detection Devices, Ltd.

Substantially Equivalent

510(k) numberK992949

Submission

Device name
Screeners Marijuana Test, Drugscreen Dip Marijuana Test
Applicant
Drug Detection Devices, Ltd.
Alpharetta, GA, US
Received
September 1, 1999
Decision date
December 27, 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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K141320LZI Oral Fluid Cannabinoids Enzyme Immunoassay, LZI Oral Fluid Cannabinoids Calibrators…LDJ · Traditional Lin-Zhi International, Inc.05/28/2015SE
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More from Healgen Scientific,, LLC

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K000452Screeners Methamphetamine Test, Drugscreen Dip Methamphetamine TestLAF · Traditional 04/24/2000SE
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K000402Screeners Phencyclidine (PCP) Test, Drugscreen Dip Phencyclidine (PCP) TestLCM · Traditional 04/18/2000SE
K000400Screeners Amphetamine Test, Drugscreen Dip Amphetamine TestDKZ · Traditional 04/18/2000SE
K000350Screeners Cocaine Test; Drugscreen Dip Cocaine TestDIO · Traditional 04/11/2000SE
K000449Screeners Benzodiazepine (BZD) Test, Drug Screen Dip Benzodiazepine (BZD) TestJXM · Traditional 04/07/2000SE
K000273Screeners Opiates Test Drugscreen Dip Opiates TestDJG · Traditional 04/07/2000SE

Questions and answers

When was Screeners Marijuana Test, Drugscreen Dip Marijuana Test cleared by the FDA?

Screeners Marijuana Test, Drugscreen Dip Marijuana Test (K992949) received a 510(k) decision of Substantially Equivalent on December 27, 1999, 117 days after the submission was received.

What is the product code of K992949?

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