510(k) K243587 ยท NFO Stimulator, Transcutaneous Electrical, Aesthetic Purposes
PureLift GLOW
| Applicant | Xtreem Pulse, LLC, New York NY, US |
| Decision | Substantially Equivalent, Mar 6, 2025 |
| Received | Nov 20, 2024 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K243587
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.