Cleared Traditional

K820198 - DERMA-AID

K820198 is an FDA 510(k) clearance for DERMA-AID, manufactured by Winfield Laboratories, Inc.. The device is a Class 1 General & Plastic Surgery device with product code NAB cleared through the Traditional 510(k) pathway after a 39-day FDA review.

K820198 · Winfield Laboratories, Inc. · General & Plastic Surgery device
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Mar 1982
Decision
39d
Days
Class 1
Risk

K820198 is an FDA 510(k) clearance for the DERMA-AID. Classified as Gauze / Sponge,nonresorbable For External Use (product code NAB), Class I - General Controls.

Submitted by Winfield Laboratories, Inc. (Mchenry, US). The FDA issued a Cleared decision on March 5, 1982 after a review of 39 days - a notably fast clearance cycle.

This device falls under the General & Plastic Surgery FDA review panel, regulated under 21 CFR 878.4014 - 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 Winfield Laboratories, Inc. devices

FDA 510(k) Submission Details - K820198

510(k) Number K820198 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received January 25, 1982
Decision Date March 05, 1982
Days to Decision 39 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
76d faster than avg
Panel avg: 115d · This submission: 39d
Pathway characteristics
Predicate-based equivalence.

NAB Device Classification - Class 1, General Controls

Product Code NAB Gauze / Sponge,nonresorbable For External Use
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 878.4014
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 - NAB Gauze / Sponge,nonresorbable For External Use

All 34
Devices cleared under the same product code (NAB) and FDA review panel - the closest regulatory comparables to K820198.
INTERSORB DRY BURN VEST & PANTS
K822047 · Chesebrough-Pond'S U.S.A. Co. · Jul 1982
UNIFLEX
K820470 · Howmedica Corp. · Jun 1982
HOLLISTER ODOR ABSORBING WOUND PAD
K820464 · Hollister, Inc. · Mar 1982
TOPPER SPONGES
K820108 · Stan-Pak Ent. · Feb 1982
TELFA STRIPS
K820056 · Stan-Pak Ent. · Feb 1982
COMBINE PAD OR ABD
K820105 · Stan-Pak Ent. · Feb 1982