510(k) K232172 ยท NFO Stimulator, Transcutaneous Electrical, Aesthetic Purposes
BTL-785BNF Handpiece
| Applicant | BTL Industries, Inc., Marlborough MA, US |
| Decision | Substantially Equivalent, Sep 18, 2023 |
| Received | Jul 21, 2023 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K232172
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.