510(k) K241748 ยท HDX Dilator, Vaginal
Intimate Rose Vaginal Dilators
| Applicant | Plus EV Holdings Dba Intimate Rose, North Kansas City MO, US |
| Decision | Substantially Equivalent, Aug 14, 2024 |
| Received | Jun 18, 2024 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K241748
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.