Cleared Traditional

K994406 - INSTANT-VIEW METHAMPHETAMINE URINE DIP ...

K994406 is the FDA 510(k) clearance for INSTANT-VIEW METHAMPHETAMINE URINE DIP ... by Alfa Scientific Designs, Inc.. It is a Class 2 Toxicology device (product code DJC) cleared through the Traditional 510(k) pathway after a 230-day FDA review.

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Aug 2000
Decision
230d
Days
Class 2
Risk

K994406 is an FDA 510(k) clearance for the INSTANT-VIEW METHAMPHETAMINE URINE DIP STRIP TEST. Classified as Thin Layer Chromatography, Methamphetamine (product code DJC), Class II - Special Controls.

Submitted by Alfa Scientific Designs, Inc. (San Diego, US). The FDA issued a Cleared decision on August 14, 2000 after a review of 230 days - an extended review cycle.

This device falls under the Toxicology FDA review panel, regulated under 21 CFR 862.3610 - 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: Standard predicate-based submission. Standard predicate reliance. This clearance follows a standard predicate-based equivalence path within the Toxicology review framework, consistent with the majority of Class II 510(k) submissions.

View all Alfa Scientific Designs, Inc. devices

Submission Details

510(k) Number K994406 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received December 28, 1999
Decision Date August 14, 2000
Days to Decision 230 days
Submission Type Traditional
Review Panel Toxicology (TX)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
143d slower than avg
Panel avg: 87d · This submission: 230d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

Product Code DJC Thin Layer Chromatography, Methamphetamine
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 862.3610
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 - DJC Thin Layer Chromatography, Methamphetamine

All 14
Devices cleared under the same product code (DJC) and FDA review panel - the closest regulatory comparables to K994406.
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WONDFO OXAZEPAM URINE TEST (BZO 200) AND WONDFO METHAMPHETAMINE URINE TEST (MET 300)
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INSTANT-VIEW MDMA (ECSTASY, XTC) URINE TEST
K022501 · Alfa Scientific Designs, Inc. · Nov 2002
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K994400 · Alfa Scientific Designs, Inc. · Aug 2000
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K001356 · Roche Diagnostics Corp. · Jul 2000
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