Cleared Traditional

K843720 - COTTON TIPPED APPLICATORS

K843720 is the FDA 510(k) clearance for COTTON TIPPED APPLICATORS by Abco Dealers, Inc.. It is a Class 1 General Hospital device (product code KXF) cleared through the Traditional 510(k) pathway after a 10-day FDA review.

K843720 · Abco Dealers, Inc. · General Hospital
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Oct 1984
Decision
10d
Days
Class 1
Risk

K843720 is an FDA 510(k) clearance for the COTTON TIPPED APPLICATORS, SINGLE. Classified as Applicator, Absorbent Tipped, Non-sterile (product code KXF), Class I - General Controls.

Submitted by Abco Dealers, Inc. (Walker, US). The FDA issued a Cleared decision on October 4, 1984 after a review of 10 days - a notably fast clearance cycle.

This device falls under the General Hospital FDA review panel, regulated under 21 CFR 880.6025 - the FDA general hospital 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 Abco Dealers, Inc. devices

Submission Details

510(k) Number K843720 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received September 24, 1984
Decision Date October 04, 1984
Days to Decision 10 days
Submission Type Traditional
Review Panel General Hospital (HO)
Summary -
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
119d faster than avg
Panel avg: 129d · This submission: 10d
Pathway characteristics
Predicate-based equivalence.

Device Classification

Product Code KXF Applicator, Absorbent Tipped, Non-sterile
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 880.6025
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 - KXF Applicator, Absorbent Tipped, Non-sterile

Devices cleared under the same product code (KXF) and FDA review panel - the closest regulatory comparables to K843720.
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