The Cellfina System— 510(k) K153677
Substantially EquivalentUlthera, Inc.
FDA 510(k) clearance K153677 for The Cellfina System, Substantially Equivalent on 2016-02-25. Applicant: Ulthera, Inc.. Device class: 2.
Clearance details
- Applicant
- Ulthera, Inc.
- Product code
- Code OUP
- Device class
- Class 2
- Regulation
- 21 CFR 878.4790
- Advisory panel
- General, Plastic Surgery
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Location
- Mesa, AZ, US
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