Cleared Traditional

K902924 - BIOSITE DIAGNOSTICS OPIATE SCREENING TEST

K902924 is the FDA 510(k) clearance for BIOSITE DIAGNOSTICS OPIATE SCREENING TEST by Biosite Incorporated. It is a Class 2 Toxicology device (product code DJG) cleared through the Traditional 510(k) pathway after a 74-day FDA review.

K902924 · Biosite Incorporated · Toxicology device
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Sep 1990
Decision
74d
Days
Class 2
Risk

K902924 is an FDA 510(k) clearance for the BIOSITE DIAGNOSTICS OPIATE SCREENING TEST. Classified as Enzyme Immunoassay, Opiates (product code DJG), Class II - Special Controls.

Submitted by Biosite Incorporated (San Diego, US). The FDA issued a Cleared decision on September 14, 1990 after a review of 74 days - a notably fast clearance cycle.

This device falls under the Toxicology FDA review panel, regulated under 21 CFR 862.3650 - 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 Biosite Incorporated devices

Submission Details

510(k) Number K902924 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received July 02, 1990
Decision Date September 14, 1990
Days to Decision 74 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
13d faster than avg
Panel avg: 87d · This submission: 74d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

Product Code DJG Enzyme Immunoassay, Opiates
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 862.3650
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 - DJG Enzyme Immunoassay, Opiates

All 136
Devices cleared under the same product code (DJG) and FDA review panel - the closest regulatory comparables to K902924.
IL TEST(TM) OPIATE
K913742 · Instrumentation Laboratory CO · Nov 1991
URINE HEROIN/MORPHINE DIRECT RIA KIT (I-125)
K913863 · Immunalysis Corporation · Sep 1991
ABUSCREEN ONLINE TM FOR OPIATES
K904997 · Roche Diagnostic Systems, Inc. · Dec 1990
EMIT(R) II OPIATE ASSAY
K902577 · Syva Co. · Jul 1990
MICRO DAU OPIATE ENZYME IMMUNOASSAY KIT
K902194 · Immunotech Corp. · Jul 1990
MILENIA(TM) OPIATES
K901577 · Diagnostic Products Corp. · May 1990