Cleared Traditional

K895764 - MODIFIED LYOFOAM WOUND DRESSINGS

K895764 is an FDA 510(k) clearance for MODIFIED LYOFOAM WOUND DRESSINGS, manufactured by Acme United Corp.. The device is a Class 1 General & Plastic Surgery device with product code KMF cleared through the Traditional 510(k) pathway after a 349-day FDA review.

K895764 · Acme United Corp. · General & Plastic Surgery device
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Sep 1990
Decision
349d
Days
Class 1
Risk

K895764 is an FDA 510(k) clearance for the MODIFIED LYOFOAM WOUND DRESSINGS. Classified as Bandage, Liquid (product code KMF), Class I - General Controls.

Submitted by Acme United Corp. (Fairfield, US). The FDA issued a Cleared decision on September 10, 1990 after a review of 349 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 880.5090 - 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. Elevated predicate reliance profile. 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 Acme United Corp. devices

FDA 510(k) Submission Details - K895764

510(k) Number K895764 FDA.gov
FDA Decision Cleared Substantially Equivalent - NSE Converted (SN)
Date Received September 26, 1989
Decision Date September 10, 1990
Days to Decision 349 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
234d slower than avg
Panel avg: 115d · This submission: 349d
Pathway characteristics
Predicate-based equivalence.

KMF Device Classification - Class 1, General Controls

Product Code KMF Bandage, Liquid
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 880.5090
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 - KMF Bandage, Liquid

All 151
Devices cleared under the same product code (KMF) and FDA review panel - the closest regulatory comparables to K895764.
ALLEVLYN WOUND DRESSING, MODIFICATION
K914147 · Smith & Nephew United, Inc. · Feb 1992
FORTEX(TM) WOUND DRESSING
K914314 · Calgon Vestal Div. · Oct 1991
INTRASITE GEL (LABELING REVISION)
K904411 · Smith & Nephew United, Inc. · Nov 1990
ALLEVYN DRESSING (LABELING REVISED)
K901877 · Smith & Nephew United, Inc. · Jun 1990
INTRASITE GEL (LABELING REVISION)
K901878 · Smith & Nephew United, Inc. · Jun 1990
FERRIS HYDROPHILIC DRESSING (ADD'L INDICATIONS)
K900127 · Ferris Mfg. Corp. · May 1990