510(k) K223595 ยท QRC Non-Implanted Electrical Stimulation Device For Management Of Premature Ejaculation
vPATCH
| Applicant | Virility Medical , Ltd., Hod-Hasharon, IL |
| Decision | Substantially Equivalent, May 1, 2023 |
| Received | Dec 2, 2022 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K223595
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.