510(k) K262861 ยท NFO Stimulator, Transcutaneous Electrical, Aesthetic Purposes
PureLift Pro Max
| Applicant | Xtreem Pulse, LLC, New York NY, US |
| Decision | Substantially Equivalent, Sep 11, 2026 |
| Received | Aug 13, 2026 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K262861
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.