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

YAG MIR II LASER

K Number: K070063 · Decision Jan 30, 2007
Classifications
1
FEI Numbers
476
Registration Numbers
479
Same Product Code
2793
Applicant Total
91
Review Days
25

Basic Information

Device Name
YAG MIR II LASER
K Number
K070063
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
878.4810
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
CYNOSURE, INC.
Date Received
January 5, 2007
Decision Date
January 30, 2007
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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