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

Harmony XL Multi-Application Platform

K Number: K181298 · Decision Jun 13, 2018
Classifications
1
FEI Numbers
92
Registration Numbers
93
Same Product Code
73
Applicant Total
20
Review Days
28

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Basic Information

Device Name
Harmony XL Multi-Application Platform
K Number
K181298
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
Alma Lasers, Inc.
Date Received
May 16, 2018
Decision Date
June 13, 2018
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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