Cleared Traditional

K932422 - 3M TEGADERM HP TRANSPARENT DRESSING

K932422 is the FDA 510(k) clearance for 3M TEGADERM HP TRANSPARENT DRESSING by 3M Health Care, Ltd.. It is a Class 1 General & Plastic Surgery device (product code KGX) cleared through the Traditional 510(k) pathway after a 222-day FDA review.

K932422 · 3M Health Care, Ltd. · General & Plastic Surgery device
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Dec 1993
Decision
222d
Days
Class 1
Risk

K932422 is an FDA 510(k) clearance for the 3M TEGADERM HP TRANSPARENT DRESSING. Classified as Tape And Bandage, Adhesive (product code KGX), Class I - General Controls.

Submitted by 3M Health Care, Ltd. (St. Paul, US). The FDA issued a Cleared decision on December 27, 1993 after a review of 222 days - an extended review cycle.

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: Standard predicate-based submission. Standard predicate reliance. This clearance follows a standard predicate-based equivalence path within the General & Plastic Surgery review framework, consistent with the majority of Class II 510(k) submissions.

View all 3M Health Care, Ltd. devices

Submission Details

510(k) Number K932422 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received May 19, 1993
Decision Date December 27, 1993
Days to Decision 222 days
Submission Type Traditional
Review Panel General & Plastic Surgery (SU)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
107d slower than avg
Panel avg: 115d · This submission: 222d
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 73
Devices cleared under the same product code (KGX) and FDA review panel - the closest regulatory comparables to K932422.
COVERLET ADHESIVE DRESSING
K940378 · Beiersdorf, Inc. · Jul 1994
CONVATEC TWO PIECE ABSORBENT DRESSING SYSTEM
K935948 · Convatec, A Division of E.R. Squibb & Sons · Mar 1994
EPISEAL ADHESIVE WOUND CLOSURE STRIPS
K935725 · Deroyal Industries, Inc. · Feb 1994
BIOCLUSIVE MVP TRANSPARENT DRESSING
K923235 · Johnson & Johnson Medical, Inc. · May 1993
STRAPPAL
K922897 · Smith & Nephew United, Inc. · Sep 1992
LUEKOFLEX SURGICAL TAPE
K923404 · Beiersdorf, Inc. · Sep 1992