Cleared Traditional

K920314 - TXIT D.A.U. BARBITURATE ASSAY (MODIFICATION)

K920314 is an FDA 510(k) clearance for TXIT D.A.U. BARBITURATE ASSAY (MODIFICA..., manufactured by Syntex Corp.. The device is a Class 2 Toxicology device with product code DIS cleared through the Traditional 510(k) pathway after a 85-day FDA review.

K920314 · Syntex Corp. · Toxicology device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Apr 1992
Decision
85d
Days
Class 2
Risk

K920314 is an FDA 510(k) clearance for the TXIT D.A.U. BARBITURATE ASSAY (MODIFICATION). Classified as Enzyme Immunoassay, Barbiturate (product code DIS), Class II - Special Controls.

Submitted by Syntex Corp. (San Jose, US). The FDA issued a Cleared decision on April 17, 1992 after a review of 85 days - a notably fast clearance cycle.

This device falls under the Toxicology FDA review panel, regulated under 21 CFR 862.3150 - 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 Syntex Corp. devices

FDA 510(k) Submission Details - K920314

510(k) Number K920314 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received January 23, 1992
Decision Date April 17, 1992
Days to Decision 85 days
Submission Type Traditional
Review Panel Toxicology (TX)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
2d faster than avg
Panel avg: 87d · This submission: 85d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

DIS Device Classification - Class 2, Special Controls

Product Code DIS Enzyme Immunoassay, Barbiturate
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 862.3150
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 - DIS Enzyme Immunoassay, Barbiturate

All 92
Devices cleared under the same product code (DIS) and FDA review panel - the closest regulatory comparables to K920314.
EMIT(R) II BARBITURATE ASSAY
K926068 · Syva Co. · Jan 1993
BARBITURATE EIA TEST
K925491 · Diagnostic Reagents, Inc. · Dec 1992
IL TEST BARBITURATE, 35289
K920417 · Instrumentation Laboratory CO · Apr 1992
DRUG OF ABUSE ANALYSIS SYSTEM
K903825 · Technicon Instruments Corp. · Sep 1990
EMIT(R) II BARBITURATE ASSAY
K902580 · Syva Co. · Jul 1990
TDX(R) BARBITURATES II ASSAY
K896550 · Abbott Laboratories · Dec 1989