Cleared Traditional

K931005 - DUKAL SKIN CLOSURE STRIP

K931005 is an FDA 510(k) clearance for DUKAL SKIN CLOSURE STRIP, manufactured by Dukal Corp.. The device is a Class 1 General & Plastic Surgery device with product code FPX cleared through the Traditional 510(k) pathway after a 138-day FDA review.

K931005 · Dukal Corp. · General & Plastic Surgery device
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Jul 1993
Decision
138d
Days
Class 1
Risk

K931005 is an FDA 510(k) clearance for the DUKAL SKIN CLOSURE STRIP. Classified as Strip, Adhesive, Closure, Skin (product code FPX), Class I - General Controls.

Submitted by Dukal Corp. (Clinton, US). The FDA issued a Cleared decision on July 14, 1993 after a review of 138 days - within the typical 510(k) review window.

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 Dukal Corp. devices

FDA 510(k) Submission Details - K931005

510(k) Number K931005 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received February 26, 1993
Decision Date July 14, 1993
Days to Decision 138 days
Submission Type Traditional
Review Panel General & Plastic Surgery (SU)
Summary Statement
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
23d slower than avg
Panel avg: 115d · This submission: 138d
Pathway characteristics
Predicate-based equivalence.

FPX Device Classification - Class 1, General Controls

Product Code FPX Strip, Adhesive, Closure, Skin
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 - FPX Strip, Adhesive, Closure, Skin

All 22
Devices cleared under the same product code (FPX) and FDA review panel - the closest regulatory comparables to K931005.
K-KLOSURE 2 INCH LENGTH/4 INCH LENGTH/8 INCH LENGTH/12 INCH LENGTH
K970441 · Medi-Flex Hospital Products, Inc. · May 1997
TECNOL SILK STRIP
K894205 · Tecnol New Jersey Wound Care, Inc. · Jul 1989
DERMA STRIP-TM SKIN CLOSURES
K833083 · Howmedica Corp. · Dec 1983
ELASTOPLAST
K831438 · Beiersdorf, Inc. · Nov 1983
ELASTOPLAST T.P.N.
K831439 · Beiersdorf, Inc. · Sep 1983
CENTRAL VENOUS CATHETER DRESSING TRAY
K802384 · American Medical Disposable, Inc. · Nov 1980