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

MODIFIED ALMA LASERS FAMILY OF ACCENT RADIOFREQUENCY (RF) SYSTEM

K Number: K101147 · Decision Jan 21, 2011
Classifications
1
FEI Numbers
20
Registration Numbers
20
Same Product Code
18
Applicant Total
20
Review Days
273

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Basic Information

Device Name
MODIFIED ALMA LASERS FAMILY OF ACCENT RADIOFREQUENCY (RF) SYSTEM
K Number
K101147
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
Alma Lasers, Inc.
Date Received
April 23, 2010
Decision Date
January 21, 2011
Product Code
NUV
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
NUV Massager, Vacuum, Light Induced Heating

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