510(k) K241617 ยท MOL Condom, Synthetic
Durex Polyisoprene Condom
| Applicant | Rb Health (Us), LLC, Parsippany NJ, US |
| Decision | Substantially Equivalent, Feb 28, 2025 |
| Received | Jun 5, 2024 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K241617
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.