Cleared Traditional

K973154 - UBI MAGIWEL MARIJUANA METABOLITES
(FDA 510(k) Clearance)

Jul 1998
Decision
334d
Days
Class 2
Risk

K973154 is an FDA 510(k) clearance for the UBI MAGIWEL MARIJUANA METABOLITES. This device is classified as a Enzyme Immunoassay, Cannabinoids (Class II - Special Controls, product code LDJ).

Submitted by United Biotech, Inc. (Mountain View, US). The FDA issued a Cleared decision on July 22, 1998, 334 days after receiving the submission on August 22, 1997.

This device falls under the Toxicology FDA review panel. Regulated under 21 CFR 862.3870.

Submission Details

510(k) Number K973154 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received August 22, 1997
Decision Date July 22, 1998
Days to Decision 334 days
Submission Type Traditional
Review Panel Toxicology (TX)
Summary Statement

Device Classification

Product Code LDJ — Enzyme Immunoassay, Cannabinoids
Device Class Class II - Special Controls
CFR Regulation 21 CFR 862.3870

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