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

PHOTOSILK PLUS PULSED LIGHT SYSTEM AND LASER ATTACHMENT

K Number: K051442 · Decision May 24, 2006
Classifications
1
FEI Numbers
476
Registration Numbers
479
Same Product Code
2793
Applicant Total
91
Review Days
356

Basic Information

Device Name
PHOTOSILK PLUS PULSED LIGHT SYSTEM AND LASER ATTACHMENT
K Number
K051442
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
878.4810
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
CYNOSURE, INC.
Date Received
June 2, 2005
Decision Date
May 24, 2006
Product Code
GEX
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
GEX Powered Laser Surgical Instrument

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