Cleared Traditional

K982493 - COMPEED PSORIASIS DRESSING

K982493 · Coloplast Corp. · General & Plastic Surgery device
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Optimized for regulatory review, auditing and printing
Jan 1999
Decision
195d
Days
-
Risk

K982493 is an FDA 510(k) clearance for the COMPEED PSORIASIS DRESSING. Classified as Dressing, Wound, Drug (product code FRO).

Submitted by Coloplast Corp. (Marietta, US). The FDA issued a Cleared decision on January 28, 1999 after a review of 195 days - an extended review cycle.

This device falls under the General & Plastic Surgery FDA review panel. 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 Coloplast Corp. devices

Submission Details

510(k) Number K982493 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received July 17, 1998
Decision Date January 28, 1999
Days to Decision 195 days
Submission Type Traditional
Review Panel General & Plastic Surgery (SU)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
80d slower than avg
Panel avg: 115d · This submission: 195d
Pathway characteristics
Predicate-based equivalence.

Device Classification

Product Code FRO Dressing, Wound, Drug
Device Class -

Regulatory Peers - FRO Dressing, Wound, Drug

All 211
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BIATAIN FOAM DRESSING
K983163 · Coloplast Corp. · Dec 1998
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K983173 · Coloplast Corp. · Dec 1998
DUODERM CGF CONTROL GEL FORMULA DRESSING
K973632 · Convatec, A Division of E.R. Squibb & Sons · Dec 1997