Cleared Traditional

K831703 - COVERUPS

K831703 is the FDA 510(k) clearance for COVERUPS by The Urology Group. It is a Class 1 General & Plastic Surgery device (product code NAD) cleared through the Traditional 510(k) pathway after a 223-day FDA review.

K831703 · The Urology Group · General & Plastic Surgery device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Jan 1984
Decision
223d
Days
Class 1
Risk

K831703 is an FDA 510(k) clearance for the COVERUPS. Classified as Dressing, Wound, Occlusive (product code NAD), Class I - General Controls.

Submitted by The Urology Group (Mchenry, US). The FDA issued a Cleared decision on January 3, 1984 after a review of 223 days - an extended review cycle.

This device falls under the General & Plastic Surgery FDA review panel, regulated under 21 CFR 878.4020 - 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 The Urology Group devices

Submission Details

510(k) Number K831703 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received May 25, 1983
Decision Date January 03, 1984
Days to Decision 223 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
108d slower than avg
Panel avg: 115d · This submission: 223d
Pathway characteristics
Predicate-based equivalence.

Device Classification

Product Code NAD Dressing, Wound, Occlusive
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 878.4020
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 - NAD Dressing, Wound, Occlusive

All 37
Devices cleared under the same product code (NAD) and FDA review panel - the closest regulatory comparables to K831703.
HYPAFIX POST OPERATIVE DRESSING
K850282 · Smith & Nephew, Inc. · May 1985
ISOLATE ADHESIVE BANDAGE FOR MOIST WOUND
K843139 · Chesebrough-Pond'S U.S.A. Co. · Nov 1984
ISOLATE ADHESIVE BANDAGE FOR DRY WOUND
K843140 · Chesebrough-Pond'S U.S.A. Co. · Nov 1984
ELASTIC BREATHABLE OVER-WRAP BANDAGE
K833729 · American Medical Disposable, Inc. · Dec 1983
LASTOBAND ADHESIVE BANDAGES
K831454 · Smith & Nephew, Inc. · Oct 1983
ENSURE DRESSING
K830593 · Warner-Lambert Co. · Apr 1983