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

REMOVE ADHESIVE REMOVER

K Number: K915150 · Decision Jan 9, 1992
Classifications
1
FEI Numbers
102
Registration Numbers
102
Same Product Code
11
Applicant Total
34
Review Days
56

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Basic Information

Device Name
REMOVE ADHESIVE REMOVER
K Number
K915150
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
878.4730
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Smith & Nephew United, Inc.
Date Received
November 14, 1991
Decision Date
January 9, 1992
Product Code
KOX
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
KOX Solvent, Adhesive Tape

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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
K935705 ALLEVYN ISLAND WOUND DRESSING
K935803 CICA-CARE SILICONE GEL SHEET
K932263 SOLOSITE DERMAL WOUND GEL
K926508 INTRASITE GEL
K922897 STRAPPAL
Search all 34 clearances from Smith & Nephew United, Inc. →