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

SIROLaser Advance+

K Number: K170500 · Decision May 16, 2017
Classifications
1
FEI Numbers
476
Registration Numbers
479
Same Product Code
2793
Applicant Total
52
Review Days
84

Basic Information

Device Name
SIROLaser Advance+
K Number
K170500
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
Dentsply Sirona
Date Received
February 21, 2017
Decision Date
May 16, 2017
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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