FDA 510(k) FDA class 1 Substantially Equivalent 🇬🇧 United Kingdom

MEDTRADE PRODUCTS SILICONE SCAR THERAPY GEL, SPENCO MEDICAL CORP. 2ND SKIN SILICONE SCAR THERAPY GEL, MODEL 09916030.

K Number: K014036 · Decision Feb 14, 2002
Classifications
1
FEI Numbers
190
Registration Numbers
190
Same Product Code
80
Applicant Total
21
Review Days
69

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Basic Information

Device Name
MEDTRADE PRODUCTS SILICONE SCAR THERAPY GEL, SPENCO MEDICAL CORP. 2ND SKIN SILICONE SCAR THERAPY GEL, MODEL 09916030.
K Number
K014036
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
Medtrade Products , Ltd.
Date Received
December 7, 2001
Decision Date
February 14, 2002
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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K093519 MEDTRADE PRODUCTS CELOX VASCULAR TOPICAL HEMOSTATIC GRANULES ON SHEET
K091795 MEDTRADE PRODUCTS CELOX TRAUMA GAUZE
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