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Variants of AURORA SR by SYNERON MEDICAL LTD
2 variants
Key
Device
Device · Manufacturer · Authorizations
Verified
Verified
Status
Status
Regime
Regime
Registry
Registry
Class
Class
Aurora Sr
Syneron Medical Ltd
·
,
FDA registration: United States
FDA 510(k)
K031993
Active
Cleared 1 Aug 2003
Active
Regimes:
510(k)
Registry:
510(k)
Class
Class:
II
Aurora Sr
Syneron Medical Ltd
·
,
FDA registration: United States
FDA 510(k)
K022266
Active
Cleared 3 Oct 2002
Active
Regimes:
510(k)
Registry:
510(k)
Class
Class:
II
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