Cleared Traditional

K011609 - LIVESURE AMPHETAMINE SCREEN TEST

K011609 is an FDA 510(k) clearance for LIVESURE AMPHETAMINE SCREEN TEST, manufactured by Pan Probe Biotech, Inc.. The device is a Class 2 Toxicology device with product code DKZ cleared through the Traditional 510(k) pathway after a 14-day FDA review.

K011609 · Pan Probe Biotech, Inc. · Toxicology device
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Jun 2001
Decision
14d
Days
Class 2
Risk

K011609 is an FDA 510(k) clearance for the LIVESURE AMPHETAMINE SCREEN TEST. Classified as Enzyme Immunoassay, Amphetamine (product code DKZ), Class II - Special Controls.

Submitted by Pan Probe Biotech, Inc. (San Diego, US). The FDA issued a Cleared decision on June 8, 2001 after a review of 14 days - a notably fast clearance cycle.

This device falls under the Toxicology FDA review panel, regulated under 21 CFR 862.3100 - 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 Pan Probe Biotech, Inc. devices

FDA 510(k) Submission Details - K011609

510(k) Number K011609 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received May 25, 2001
Decision Date June 08, 2001
Days to Decision 14 days
Submission Type Traditional
Review Panel Toxicology (TX)
Summary Summary PDF
Third-party Review Yes - reviewed by an FDA-accredited third party
Regulatory Context
Review time vs. panel average
73d faster than avg
Panel avg: 87d · This submission: 14d
Pathway characteristics
Predicate-based equivalence. No clinical trials required. Third-party reviewed.

DKZ Device Classification - Class 2, Special Controls

Product Code DKZ Enzyme Immunoassay, Amphetamine
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 862.3100
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 - DKZ Enzyme Immunoassay, Amphetamine

All 197
Devices cleared under the same product code (DKZ) and FDA review panel - the closest regulatory comparables to K011609.
ACON AMP ONE STEP AMPHETAMINE TEST STRIP, ACON AMP ONE STEP AMPHETAMINE TEST DEVICE
K011673 · ACON Laboratories, Inc. · Jul 2001
RAPID DRUG SCREEN
K012159 · American Bio Medica Corp. · Jul 2001
VISUALINE AMPHETAMINE DIPSTRIP ASSAY
K011499 · Sun Biomedical Laboratories, Inc. · Jul 2001
VISUALINE II (ALSO KNOWN AS SUNLINE) AMPHETAMINE ASSAY
K010177 · Sun Biomedical Laboratories, Inc. · May 2001
VERDICT -II THC/COC/OPI/AMP/PCP/BAR/BZO & THC/COC/BAR/BZO
K010564 · Medtox Diagnostics, Inc. · Apr 2001
AT HOME DRUG TEST, MODEL 9063 T
K010645 · Phamatech · Mar 2001