510(k) K221443 ยท NFO Stimulator, Transcutaneous Electrical, Aesthetic Purposes
PureLift Pro Plus
| Applicant | Xtreem Pulse, LLC, New York NY, US |
| Decision | Substantially Equivalent, Oct 21, 2022 |
| Received | May 18, 2022 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K221443
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.