Cleared Traditional

K874213 - ACA DU PONT URINE COCAINE METABOLITE (U...

K874213 is the FDA 510(k) clearance for ACA DU PONT URINE COCAINE METABOLITE (U... by E.I. Dupont DE Nemours & Co., Inc.. It is a Class 2 Toxicology device (product code DIO) cleared through the Traditional 510(k) pathway after a 28-day FDA review.

K874213 · E.I. Dupont DE Nemours & Co., Inc. · Toxicology device
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Nov 1987
Decision
28d
Days
Class 2
Risk

K874213 is an FDA 510(k) clearance for the ACA DU PONT URINE COCAINE METABOLITE (U COC)SCREEN. Classified as Enzyme Immunoassay, Cocaine And Cocaine Metabolites (product code DIO), Class II - Special Controls.

Submitted by E.I. Dupont DE Nemours & Co., Inc. (Wilmington, US). The FDA issued a Cleared decision on November 13, 1987 after a review of 28 days - a notably fast clearance cycle.

This device falls under the Toxicology FDA review panel, regulated under 21 CFR 862.3250 - the FDA toxicology device framework. The Traditional 510(k) pathway establishes clearance through substantial equivalence to a legally marketed predicate device, without requiring clinical trial data.

Device pattern: Fast-track predicate clearance. Standard predicate reliance. The short review cycle indicates strong predicate alignment - the FDA found sufficient equivalence without extended technical review.

View all E.I. Dupont DE Nemours & Co., Inc. devices

Submission Details

510(k) Number K874213 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received October 16, 1987
Decision Date November 13, 1987
Days to Decision 28 days
Submission Type Traditional
Review Panel Toxicology (TX)
Summary -
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
59d faster than avg
Panel avg: 87d · This submission: 28d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

Product Code DIO Enzyme Immunoassay, Cocaine And Cocaine Metabolites
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 862.3250
What this classification means

Class II devices require demonstration of substantial equivalence to a legally marketed predicate device. This pathway does not require clinical trials - it relies on engineering equivalence and performance data. Most Toxicology devices follow this clearance model.

Regulatory Peers - DIO Enzyme Immunoassay, Cocaine And Cocaine Metabolites

All 82
Devices cleared under the same product code (DIO) and FDA review panel - the closest regulatory comparables to K874213.
EMIT HVA COCAINE METABOLITE ASSAY
K881942 · Syva Co. · Jul 1988
REVISED LABELING FOR ADX COCAINE METABOLITE
K880009 · Abbott Laboratories · Mar 1988
REVISED LABELING FOR TDX COCAINE METABOLITE
K874487 · Abbott Laboratories · Nov 1987
REVISED LABELING FOR COCAINE/COCAINE META. TEST
K874271 · Roche Diagnostic Systems, Inc. · Nov 1987
REVISED LABELING FOR SYVA COCAINE METABOLITE ASSAY
K874201 · Syva Co. · Oct 1987
LABELING CHANGE COAT-A-COUNT COCAINE METABOLITE
K873751 · Diagnostic Products Corp. · Oct 1987