Cleared Traditional

K971218 - QUIKSTRIP ONE STEP AMPHETAMINE TEST

K971218 is an FDA 510(k) clearance for QUIKSTRIP ONE STEP AMPHETAMINE TEST, manufactured by Drial Consultants, Inc.. The device is a Class 2 Toxicology device with product code DKZ cleared through the Traditional 510(k) pathway after a 58-day FDA review.

K971218 · Drial Consultants, Inc. · Toxicology device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
May 1997
Decision
58d
Days
Class 2
Risk

K971218 is an FDA 510(k) clearance for the QUIKSTRIP ONE STEP AMPHETAMINE TEST. Classified as Enzyme Immunoassay, Amphetamine (product code DKZ), Class II - Special Controls.

Submitted by Drial Consultants, Inc. (Simi Valley, US). The FDA issued a Cleared decision on May 30, 1997 after a review of 58 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 Drial Consultants, Inc. devices

FDA 510(k) Submission Details - K971218

510(k) Number K971218 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received April 02, 1997
Decision Date May 30, 1997
Days to Decision 58 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
29d faster than avg
Panel avg: 87d · This submission: 58d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

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 186
Devices cleared under the same product code (DKZ) and FDA review panel - the closest regulatory comparables to K971218.
ABUSCREEN ONLINE FOR AMPHETAMINES WITH PERIODATE - OLYMPUS AU800/1000 INSTRUMENT APPLICATION
K972891 · Roche Diagnostic Systems, Inc. · Oct 1997
VISUALINE II METHAMPHETIMINE
K972032 · Sun Biomedical Laboratories, Inc. · Aug 1997
QUIKSTRIP ONE STEP METHAMPHETAMINE
K970395 · Drial Consultants, Inc. · Jun 1997
QUIKPAC II ONE STEP AMPHETAMINE TEST
K971109 · Drial Consultants, Inc. · May 1997
QUICKPAC II ONE STEP METHAMPHETAMINE TEST
K970724 · Drial Consultants, Inc. · May 1997
ONE STEP URINE DRUG OF ABUSE METHAMPHETAMINE TEST
K970265 · Drial Consultants, Inc. · Apr 1997