Cleared Traditional

K961724 - U-DOA CONTROLS

K961724 is the FDA 510(k) clearance for U-DOA CONTROLS by Medical Diagnostic Technologies, Inc.. It is a Class 1 Toxicology device (product code DIF) cleared through the Traditional 510(k) pathway after a 31-day FDA review.

K961724 · Medical Diagnostic Technologies, Inc. · Toxicology device
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Jun 1996
Decision
31d
Days
Class 1
Risk

K961724 is an FDA 510(k) clearance for the U-DOA CONTROLS. Classified as Drug Mixture Control Materials (product code DIF), Class I - General Controls.

Submitted by Medical Diagnostic Technologies, Inc. (Ventura, US). The FDA issued a Cleared decision on June 3, 1996 after a review of 31 days - a notably fast clearance cycle.

This device falls under the Toxicology FDA review panel, regulated under 21 CFR 862.3280 - 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 Medical Diagnostic Technologies, Inc. devices

Submission Details

510(k) Number K961724 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received May 03, 1996
Decision Date June 03, 1996
Days to Decision 31 days
Submission Type Traditional
Review Panel Toxicology (TX)
Summary Statement
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
56d faster than avg
Panel avg: 87d · This submission: 31d
Pathway characteristics
Predicate-based equivalence.

Device Classification

Product Code DIF Drug Mixture Control Materials
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 862.3280
What this classification means

Class I devices are subject to general controls only and most are exempt from 510(k) premarket notification. They represent the lowest regulatory burden in the FDA device framework.

Regulatory Peers - DIF Drug Mixture Control Materials

All 147
Devices cleared under the same product code (DIF) and FDA review panel - the closest regulatory comparables to K961724.
CEDIA DAU MULTI-DRUG CONTROL CEDIA DAU SPECIALTY CONTROL SET 1
K965157 · Boehringer Mannheim Corp. · Jan 1997
ONTRAK TESTTCUP COLLECTION/URINALYSIS PANEL
K964422 · Roche Diagnostic Systems, Inc. · Nov 1996
COBAS-FP TDM CALIBRATION VERIFICATION TEST SET
K962165 · Roche Diagnostic Systems, Inc. · Jun 1996
DOCUMENT TDM ULTRA ASSAYED CONTROL
K960244 · Casco Standards · Mar 1996
LYPHOCHEK BENZO/TCA CONTROL-SET B
K955153 · Bio-Rad · Feb 1996
DOCUMENT TDM ULTRA UNASSAYED CONTROL
K955155 · Casco Standards · Dec 1995