510(k) K241897 ยท QRC Non-Implanted Electrical Stimulation Device For Management Of Premature Ejaculation
MOR
| Applicant | Morari, Inc., Maple Grove MN, US |
| Decision | Substantially Equivalent, Feb 11, 2025 |
| Received | Jun 28, 2024 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K241897
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.