Cleared Traditional

K833580 - MODIF. OF EMIT URINE CANNABINOID (FDA 510(k) Clearance)

Jan 1984
Decision
106d
Days
Class 2
Risk

K833580 is an FDA 510(k) clearance for the MODIF. OF EMIT URINE CANNABINOID. This device is classified as a Enzyme Immunoassay, Cannabinoids (Class II - Special Controls, product code LDJ).

Submitted by Syva Co. (Mchenry, US). The FDA issued a Cleared decision on January 26, 1984, 106 days after receiving the submission on October 12, 1983.

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

Submission Details

510(k) Number K833580 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received October 12, 1983
Decision Date January 26, 1984
Days to Decision 106 days
Submission Type Traditional
Review Panel Toxicology (TX)
Summary

Device Classification

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

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