FDA 510(k) Applications Submitted by Ulthera, Inc
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K180623 | 03/09/2018 | Ulthera System | Ulthera, Inc |
| K192185 | 08/12/2019 | The Cellfina System | Ulthera, Inc |
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