Cleared Traditional

K910892 - TARGET(TM) CANNABINOIDS-V TEST

K910892 is the FDA 510(k) clearance for TARGET(TM) CANNABINOIDS-V TEST by V-Tech, Inc.. It is a Class 2 Toxicology device (product code LDJ) cleared through the Traditional 510(k) pathway after a 30-day FDA review.

K910892 · V-Tech, Inc. · Toxicology device
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Apr 1991
Decision
30d
Days
Class 2
Risk

K910892 is an FDA 510(k) clearance for the TARGET(TM) CANNABINOIDS-V TEST. Classified as Enzyme Immunoassay, Cannabinoids (product code LDJ), Class II - Special Controls.

Submitted by V-Tech, Inc. (El Monte, US). The FDA issued a Cleared decision on April 3, 1991 after a review of 30 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 V-Tech, Inc. devices

Submission Details

510(k) Number K910892 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received March 04, 1991
Decision Date April 03, 1991
Days to Decision 30 days
Submission Type Traditional
Review Panel Toxicology (TX)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
57d faster than avg
Panel avg: 87d · This submission: 30d
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 86
Devices cleared under the same product code (LDJ) and FDA review panel - the closest regulatory comparables to K910892.
ABUSCREEN RADIOIMMUNOASSAY FOR CANNABINIODS
K912757 · Roche Diagnostic Systems, Inc. · Jul 1991
ABUSCREEN FP FOR CANNABINOIDS (15-50)
K910592 · Roche Diagnostic Systems, Inc. · Jun 1991
ABUSCREEN FP FOR CANNABINOIDS (50-100)
K910589 · Roche Diagnostic Systems, Inc. · Apr 1991
EMIT(R) II CANNABINOID 100 NG ASSAY
K904568 · Syva Co. · Dec 1990
EMIT(R) II CANNABINOID 20 NG ASSAY
K904570 · Syva Co. · Dec 1990
EMIT(R) II CANNABINOID 50 NG ASSAY
K904571 · Syva Co. · Dec 1990