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

ADVERL EVO ER: YAG LASER FOR DENTISTRY MEY-1-A

K Number: K120377 · Decision Jul 25, 2012
Classifications
1
FEI Numbers
476
Registration Numbers
479
Same Product Code
2793
Applicant Total
47
Review Days
170

Basic Information

Device Name
ADVERL EVO ER: YAG LASER FOR DENTISTRY MEY-1-A
K Number
K120377
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
J. MORITA USA, INC.
Date Received
February 6, 2012
Decision Date
July 25, 2012
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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