FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

SMOOTHCOOL

K Number: K092326 · Decision Mar 5, 2010
Classifications
1
FEI Numbers
92
Registration Numbers
93
Same Product Code
73
Applicant Total
15
Review Days
213

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Basic Information

Device Name
SMOOTHCOOL
K Number
K092326
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
878.4810
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Jeisys Medical, Inc.
Date Received
August 4, 2009
Decision Date
March 5, 2010
Product Code
ONF
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
ONF Powered Light Based Non-Laser Surgical Instrument With Thermal Effect

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