Cleared Traditional

K952526 - CUTINOVA CAVITY

K952526 is an FDA 510(k) clearance for CUTINOVA CAVITY, manufactured by Beiersdorf, Inc.. The device is a Class 1 General & Plastic Surgery device with product code KMF cleared through the Traditional 510(k) pathway after a 74-day FDA review.

K952526 · Beiersdorf, Inc. · General & Plastic Surgery device
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Aug 1995
Decision
74d
Days
Class 1
Risk

K952526 is an FDA 510(k) clearance for the CUTINOVA CAVITY. Classified as Bandage, Liquid (product code KMF), Class I - General Controls.

Submitted by Beiersdorf, Inc. (Norwalk, US). The FDA issued a Cleared decision on August 14, 1995 after a review of 74 days - a notably fast clearance cycle.

This device falls under the General & Plastic Surgery FDA review panel, regulated under 21 CFR 880.5090 - 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 Beiersdorf, Inc. devices

FDA 510(k) Submission Details - K952526

510(k) Number K952526 FDA.gov
FDA Decision Cleared Substantially Equivalent - NSE Converted (SN)
Date Received June 01, 1995
Decision Date August 14, 1995
Days to Decision 74 days
Submission Type Traditional
Review Panel General & Plastic Surgery (SU)
Summary -
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
41d faster than avg
Panel avg: 115d · This submission: 74d
Pathway characteristics
Predicate-based equivalence.

KMF Device Classification - Class 1, General Controls

Product Code KMF Bandage, Liquid
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 880.5090
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 - KMF Bandage, Liquid

All 73
Devices cleared under the same product code (KMF) and FDA review panel - the closest regulatory comparables to K952526.
COMFEEL:ALGINATE DRESSING
K953497 · Coloplast A/S · Sep 1995
HYDROPHILIC FOAM DRESSING
K953019 · Busse Hospital Disposables, Inc. · Sep 1995
WOUNDFOAM 4 X 4
K953070 · Trinity Laboratories, Inc. · Sep 1995
CURASORB ZN ALGINATE WOUND DRESSING
K950775 · Kendall Healthcare Products Co. Div.Of Tyco Health · Apr 1995
ALLEVYN ADHESIVE
K945330 · Smith & Nephew United, Inc. · Feb 1995
CURAFOAM ANDD CURAFOAM PLUS HYDROPHILIC POLYURETHANE FOAM DRESSINGS
K946269 · Kendall Healthcare Products Co. Div.Of Tyco Health · Jan 1995