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

MENTOR H/S SILICONE GEL SHEETING FOR SCAR MANAGEMENT

K Number: K962013 · Decision Aug 22, 1996
Classifications
1
FEI Numbers
183
Registration Numbers
183
Same Product Code
80
Applicant Total
61
Review Days
91

Basic Information

Device Name
MENTOR H/S SILICONE GEL SHEETING FOR SCAR MANAGEMENT
K Number
K962013
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
878.4025
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
MENTOR CORP.
Date Received
May 23, 1996
Decision Date
August 22, 1996
Product Code
MDA
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
MDA Elastomer, Silicone, For Scar Management

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K042851 MENTOR OBTAPE TRANS-OBTURATOR SURGICAL KIT
K040959 MENTOR GENESIS PENILE PROSTHESIS
K031767 MENTOR OBTAPE TRANS-OBTURATOR TAPE
K011493 MENTOR ISOLOADER AUTOMATIC NEEDLE LOADING SYSTEM AND PHYSICS WORKSTATION FOR BRACHYTHERAPY
K011500 MENTOR CONTOUR PROFILE TISSUE EXPANDER
K004005 MENTOR ULTRASOUND-ASSISTED TISSUE REMOVAL SYSTEM (CURRENT), MENTOR CONTOUR GENESIS SYSTEM (PROPOSED)
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