Quickpac II One Step Marijuana (THC) Test

FDA 510(k) K963207 · Drial Consultants, Inc.

Substantially Equivalent

510(k) numberK963207

Submission

Device name
Quickpac II One Step Marijuana (THC) Test
Applicant
Drial Consultants, Inc.
Menlo Park, CA, US
Received
August 15, 1996
Decision date
February 20, 1997
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

510(k)DeviceDecision
K973269Quikstrip One Step Benzodiazepine TestJXM · Traditional 02/25/1998SE
K973326Quikpac II One Step Benzodiazepine TestJXM · Traditional 02/24/1998SE
K973047One Step Urine Drug of Abuse Barbiturate TestDIS · Traditional 10/02/1997SE
K972059Quikpac II One Step Cocaine TestDIO · Traditional 08/28/1997SE
K972571Quikstrip One Step Opiates TestDJG · Traditional 08/20/1997SE
K972405Quikpac II One Step Opiate TestDJG · Traditional 08/08/1997SE
K971926Quikstrip One Step Cocaine TestDIO · Traditional 07/14/1997SE
K970395Quikstrip One Step MethamphetamineDKZ · Traditional 06/26/1997SE
K971218Quikstrip One Step Amphetamine TestDKZ · Traditional 05/30/1997SE
K971109Quikpac II One Step Amphetamine TestDKZ · Traditional 05/14/1997SE

Questions and answers

When was Quickpac II One Step Marijuana (THC) Test cleared by the FDA?

Quickpac II One Step Marijuana (THC) Test (K963207) received a 510(k) decision of Substantially Equivalent on February 20, 1997, 189 days after the submission was received.

What is the product code of K963207?

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