Cleared Traditional

K841533 - ACA TRICYCLIC ANTIDEPRESSANTS SCREEN (FDA 510(k) Clearance)

Class I Toxicology device.

K841533 · E.I. Dupont DE Nemours & Co., Inc. · Toxicology device
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May 1984
Decision
25d
Days
Class 1
Risk

K841533 is an FDA 510(k) clearance for the ACA TRICYCLIC ANTIDEPRESSANTS SCREEN. Classified as Drug Specific Control Materials (product code LAS), Class I - General Controls.

Submitted by E.I. Dupont DE Nemours & Co., Inc. (Walker, US). The FDA issued a Cleared decision on May 11, 1984 after a review of 25 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 E.I. Dupont DE Nemours & Co., Inc. devices

Submission Details

510(k) Number K841533 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received April 16, 1984
Decision Date May 11, 1984
Days to Decision 25 days
Submission Type Traditional
Review Panel Toxicology (TX)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
62d faster than avg
Panel avg: 87d · This submission: 25d
Pathway characteristics
Predicate-based equivalence.

Device Classification

Product Code LAS Drug Specific 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.