Cleared Traditional

K874813 - OMED WOUND CLOSURE STRIPS

K874813 is an FDA 510(k) clearance for OMED WOUND CLOSURE STRIPS, manufactured by Oxboro Medical Intl., Inc.. The device is a Class 1 General & Plastic Surgery device with product code FPX cleared through the Traditional 510(k) pathway after a 66-day FDA review.

K874813 · Oxboro Medical Intl., Inc. · General & Plastic Surgery device
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Jan 1988
Decision
66d
Days
Class 1
Risk

K874813 is an FDA 510(k) clearance for the OMED WOUND CLOSURE STRIPS. Classified as Strip, Adhesive, Closure, Skin (product code FPX), Class I - General Controls.

Submitted by Oxboro Medical Intl., Inc. (Bloomington, US). The FDA issued a Cleared decision on January 29, 1988 after a review of 66 days - a notably fast clearance 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: Fast-track predicate clearance. Standard predicate reliance. The short review cycle indicates strong predicate alignment - the FDA found sufficient equivalence without extended technical review.

View all Oxboro Medical Intl., Inc. devices

FDA 510(k) Submission Details - K874813

510(k) Number K874813 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received November 24, 1987
Decision Date January 29, 1988
Days to Decision 66 days
Submission Type Traditional
Review Panel General & Plastic Surgery (SU)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
49d faster than avg
Panel avg: 115d · This submission: 66d
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 K874813.
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K831439 · Beiersdorf, Inc. · Sep 1983
CENTRAL VENOUS CATHETER DRESSING TRAY
K802384 · American Medical Disposable, Inc. · Nov 1980