510(k) K190269 ยท NFO Stimulator, Transcutaneous Electrical, Aesthetic Purposes
PureLift
| Applicant | Xtreem Pulse, LLC, New York NY, US |
| Decision | Substantially Equivalent, Aug 28, 2019 |
| Received | Feb 8, 2019 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K190269
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.