FDA 510(k) FDA class 2 Substantially Equivalent 🇮🇱 Israel

VELASHAPE

K Number: K122579 · Decision Sep 13, 2012
Classifications
1
FEI Numbers
20
Registration Numbers
20
Same Product Code
18
Applicant Total
35
Review Days
21

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Basic Information

Device Name
VELASHAPE
K Number
K122579
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
Syneron Medical, Ltd.
Date Received
August 23, 2012
Decision Date
September 13, 2012
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

Similar 510(k) Clearances

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Other Clearances by Syneron Medical, Ltd.

K Number Device Name
K170370 ULTRASHAPE POWER SYSTEM
K163415 SlimShape System
K162163 UltraShape System
K161952 UltraShape System
K160896 ULTRASHAPE POWER SYSTEM
K151655 CO2RE System
K141507 TWO SKIN TREATMENT SYSTEM
K141708 ULTRASHAPE SYSTEM
K133238 CONTOUR I V3.1 SYSTEM
K120510 TRANSCEND
Search all 35 clearances from Syneron Medical, Ltd. →