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Variants of VELASHAPE by SYNERON MEDICAL LTD
2 variants
Key
Device
Device · Manufacturer · Authorizations
Verified
Verified
Status
Status
Regime
Regime
Registry
Registry
Class
Class
Velashape
Syneron Medical Ltd
·
,
FDA registration: United States
FDA 510(k)
K071872
Active
Cleared 22 Aug 2007
Active
Regimes:
510(k)
Registry:
510(k)
Class
Class:
II
Velashape
Syneron Medical Ltd
·
,
FDA registration: United States
FDA 510(k)
K122579
Active
Cleared 13 Sep 2012
Active
Regimes:
510(k)
Registry:
510(k)
Class
Class:
II
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