FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

ALLEVYN ISLAND WOUND DRESSING

K Number: K935705 · Decision Feb 15, 1994
Classifications
1
FEI Numbers
292
Registration Numbers
292
Same Product Code
28
Applicant Total
34
Review Days
77

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Basic Information

Device Name
ALLEVYN ISLAND WOUND DRESSING
K Number
K935705
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
878.4022
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Smith & Nephew United, Inc.
Date Received
November 30, 1993
Decision Date
February 15, 1994
Product Code
NAE
Advisory Committee
General, Plastic Surgery
Review Advisory Committee
SU
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
NAE Dressing, Wound, Hydrogel Without Drug And/Or Biologic

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (NAE), ordered by most recent decision date.

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Other Clearances by Smith & Nephew United, Inc.

K Number Device Name
K963096 ALLEVYN HYDRO POLY DRESSING ND ALL TRAC DRESSING
K961775 PROFORE FOUR-LAYER BANDAGE SYSTEM KIT
K945330 ALLEVYN ADHESIVE
K943619 CAVI-CARE CONFORMING FOAM DRESSING
K942748 INTRASITE
K935803 CICA-CARE SILICONE GEL SHEET
K932263 SOLOSITE DERMAL WOUND GEL
K926508 INTRASITE GEL
K922897 STRAPPAL
K914147 ALLEVLYN WOUND DRESSING, MODIFICATION
Search all 34 clearances from Smith & Nephew United, Inc. →