Cleared Traditional

K813265 - 3M STERI-STRIP ANTIMICROBIAL SKIN CLOS

K813265 is an FDA 510(k) clearance for 3M STERI-STRIP ANTIMICROBIAL SKIN CLOS, manufactured by 3M Company. The device is a Class 1 General & Plastic Surgery device with product code KGX cleared through the Traditional 510(k) pathway after a 446-day FDA review.

K813265 · 3M Company · General & Plastic Surgery device
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Feb 1983
Decision
446d
Days
Class 1
Risk

K813265 is an FDA 510(k) clearance for the 3M STERI-STRIP ANTIMICROBIAL SKIN CLOS. Classified as Tape And Bandage, Adhesive (product code KGX), Class I - General Controls.

Submitted by 3M Company (White City, US). The FDA issued a Cleared decision on February 9, 1983 after a review of 446 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.

FDA 510(k) Submission Details - K813265

510(k) Number K813265 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received November 20, 1981
Decision Date February 09, 1983
Days to Decision 446 days
Submission Type Traditional
Review Panel General & Plastic Surgery (SU)
Summary -
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
331d slower than avg
Panel avg: 115d · This submission: 446d
Pathway characteristics
Predicate-based equivalence.

KGX Device Classification - Class 1, General Controls

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 K813265.
ONE TIME COMPOUND BENZOIN TINCTURE-
K833120 · Acme United Corp. · Dec 1983
SYSTENET
K832544 · American Intl. Medical Supply Co. · Nov 1983
ADHESIVE TAPE/FIRST-BAND
K822824 · Leonard Joseph Co. · Jun 1983
SATOBAN FIRST AID TAPE
K823076 · Food and Drug Service, Inc. · Jan 1983
SILKAFIX ADHESIVE PLASTER
K821490 · Selomas, Inc. · Jun 1982
SELOFIX
K821257 · Selomas, Inc. · May 1982
K813265 · 3M STERI-STRIP ANTIMICROBIAL SKIN CLOS
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