510(k) K241832 ยท GEI Electrosurgical, Cutting & Coagulation & Accessories
Unicorn+ RF System (Unicorn+); Unicorn+ RF System (Unicorn+ I); Unicorn+ RF System (Unicorn+ II); Unicorn+ RF System (Unicorn+ III)
| Applicant | Boston Aesthetics, Inc., Wilmington DE, US |
| Decision | Substantially Equivalent, Feb 13, 2025 |
| Received | Jun 25, 2024 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K241832
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.