Cleared Traditional

ADHESIVE BANDAGES WITH OTC DRUG (K943314) - FDA 510(k) Clearance

Class I General & Plastic Surgery device.

K943314 · Johnson & Johnson Consumer Products, Inc. · General & Plastic Surgery device
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Optimized for regulatory review, auditing and printing
Jan 1996
Decision
555d
Days
Class 1
Risk

K943314 is an FDA 510(k) clearance for the ADHESIVE BANDAGES WITH OTC DRUG. Classified as Tape And Bandage, Adhesive (product code KGX), Class I - General Controls.

Submitted by Johnson & Johnson Consumer Products, Inc. (Skillman, US). The FDA issued a Cleared decision on January 17, 1996 after a review of 555 days - an unusually long review period, suggesting complex equivalence evaluation.

This device falls under the General & Plastic Surgery FDA review panel, regulated under 21 CFR 880.5240 - the FDA general and plastic surgery 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: High-complexity regulatory submission. Elevated predicate reliance profile. The extended review timeline suggests the FDA required additional documentation before confirming substantial equivalence - a pattern common in complex or first-of-kind General & Plastic Surgery submissions.

View all Johnson & Johnson Consumer Products, Inc. devices

Submission Details

510(k) Number K943314 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received July 11, 1994
Decision Date January 17, 1996
Days to Decision 555 days
Submission Type Traditional
Review Panel General & Plastic Surgery (SU)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
440d slower than avg
Panel avg: 115d · This submission: 555d
Pathway characteristics
Predicate-based equivalence.

Device Classification

Product Code KGX Tape And Bandage, Adhesive
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 880.5240
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 - KGX Tape And Bandage, Adhesive

All 186
Devices cleared under the same product code (KGX) and FDA review panel - the closest regulatory comparables to K943314.
STERILE PLASTIC DRESSING
K944588 · Smith & Nephew, Inc. · Nov 1994
PROMEON HYDROGEL DRESSING #45 NONSTERILE W/ MESH
K915358 · Medtronic Vascular · Apr 1992
3M FIRST AID BANDAGE FOR MINOR WOUNDS
K901777 · 3M Company · Aug 1990
TEGADERM BRAND TRANSPARENT DRESSING SERIES 16XX
K901845 · 3M Company · Jul 1990
DERMASTRIP
K883660 · Bd Becton Dickinson Vacutainer Systems Preanalytic · Feb 1989
MELOLITE
K833954 · Smith & Nephew, Inc. · Mar 1984