ULTRASHAPE SYSTEM— 510(k) K141708
Substantially EquivalentSyneron Medical, Ltd.
FDA 510(k) clearance K141708 for ULTRASHAPE SYSTEM, Substantially Equivalent on 2014-10-06. Applicant: Syneron Medical, Ltd.. Device class: 2.
Clearance details
- Applicant
- Syneron Medical, Ltd.
- Product code
- Product code OHV
- Device class
- Class 2
- Regulation
- 21 CFR 878.4590
- Advisory panel
- General, Plastic Surgery
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Philedelphia, PA, US
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