Cleared Traditional

K952738 - SKIN SAVER SYSTEMS

K952738 is an FDA 510(k) clearance for SKIN SAVER SYSTEMS, manufactured by Skin Saver Systems, Inc.. The device is a Class 1 General Hospital device with product code FQM cleared through the Traditional 510(k) pathway after a 107-day FDA review.

K952738 · Skin Saver Systems, Inc. · General Hospital
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Sep 1995
Decision
107d
Days
Class 1
Risk

K952738 is an FDA 510(k) clearance for the SKIN SAVER SYSTEMS. Classified as Bandage, Elastic (product code FQM), Class I - General Controls.

Submitted by Skin Saver Systems, Inc. (Aurora, US). The FDA issued a Cleared decision on September 29, 1995 after a review of 107 days - within the typical 510(k) review window.

This device falls under the General Hospital FDA review panel, regulated under 21 CFR 880.5075 - the FDA general hospital 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 Hospital review framework, consistent with the majority of Class II 510(k) submissions.

View all Skin Saver Systems, Inc. devices

FDA 510(k) Submission Details - K952738

510(k) Number K952738 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received June 14, 1995
Decision Date September 29, 1995
Days to Decision 107 days
Submission Type Traditional
Review Panel General Hospital (HO)
Summary Statement
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
22d faster than avg
Panel avg: 129d · This submission: 107d
Pathway characteristics
Predicate-based equivalence.

FQM Device Classification - Class 1, General Controls

Product Code FQM Bandage, Elastic
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 880.5075
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 - FQM Bandage, Elastic

All 21
Devices cleared under the same product code (FQM) and FDA review panel - the closest regulatory comparables to K952738.
ASPEN ESMARK BANDAGE
K872868 · Aspen Laboratories, Inc. · Jul 1987
COMPRESSOGRIP TUBULAR ELASTIC BANDAGE
K831551 · Fred Sammons, Inc. · Jun 1983
BIAS STOCKINETTE
K820141 · Stan-Pak Ent. · Feb 1982
TUBULAR STOCKINETTE
K820142 · Stan-Pak Ent. · Feb 1982
ELASTIC BANDAGE
K820094 · Stan-Pak Ent. · Jan 1982
SOF-BAND HIGH STRETCH BANDAGES
K810137 · Johnson & Johnson Professionals, Inc. · Feb 1981