Cleared Traditional

BECKMAN CX AMMONIA/ALCOHOL CONTROL (K934467) - FDA 510(k) Clearance

Class I Toxicology device.

K934467 · Beckman-Diagnostic Systems Group · Toxicology device
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Oct 1993
Decision
47d
Days
Class 1
Risk

K934467 is an FDA 510(k) clearance for the BECKMAN CX AMMONIA/ALCOHOL CONTROL. Classified as Alcohol Control Materials (product code DKC), Class I - General Controls.

Submitted by Beckman-Diagnostic Systems Group (Brea, US). The FDA issued a Cleared decision on October 27, 1993 after a review of 47 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 Beckman-Diagnostic Systems Group devices

Submission Details

510(k) Number K934467 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received September 10, 1993
Decision Date October 27, 1993
Days to Decision 47 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
40d faster than avg
Panel avg: 87d · This submission: 47d
Pathway characteristics
Predicate-based equivalence.

Device Classification

Product Code DKC Alcohol 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.