Cleared Traditional

K875252 - ACA DU PONT URINE CANNABINOIDS (U THC) ...

K875252 is the FDA 510(k) clearance for ACA DU PONT URINE CANNABINOIDS (U THC) ... by E.I. Dupont DE Nemours & Co., Inc.. It is a Class 2 Toxicology device (product code LDJ) cleared through the Traditional 510(k) pathway after a 43-day FDA review.

K875252 · E.I. Dupont DE Nemours & Co., Inc. · Toxicology device
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Feb 1988
Decision
43d
Days
Class 2
Risk

K875252 is an FDA 510(k) clearance for the ACA DU PONT URINE CANNABINOIDS (U THC) SCREEN METH. Classified as Enzyme Immunoassay, Cannabinoids (product code LDJ), Class II - Special Controls.

Submitted by E.I. Dupont DE Nemours & Co., Inc. (Wilmington, US). The FDA issued a Cleared decision on February 3, 1988 after a review of 43 days - a notably fast clearance cycle.

This device falls under the Toxicology FDA review panel, regulated under 21 CFR 862.3870 - 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 K875252 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received December 22, 1987
Decision Date February 03, 1988
Days to Decision 43 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
44d faster than avg
Panel avg: 87d · This submission: 43d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

Product Code LDJ Enzyme Immunoassay, Cannabinoids
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 862.3870
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 - LDJ Enzyme Immunoassay, Cannabinoids

All 85
Devices cleared under the same product code (LDJ) and FDA review panel - the closest regulatory comparables to K875252.
EMIT HVA CANNABINOID 100 NG ASSAY
K882819 · Syva Co. · Aug 1988
ABUSCREEN(R) ONTRAK(TM) FOR THC
K881814 · Roche Diagnostic Systems, Inc. · Jul 1988
REVISED LABELING FOR ADX CANNABINOIDS
K880015 · Abbott Laboratories · Mar 1988
TDXR DELTA-9-CANNABINOIDS
K874646 · Abbott Laboratories · Dec 1987
REVISED LABELING FOR TDX CANNABINOIDS
K874488 · Abbott Laboratories · Nov 1987
REVISED LABELING FOR CANNABINOIDS TEST KIT
K874269 · Roche Diagnostic Systems, Inc. · Nov 1987