510(k) K200672 ยท HIS Condom
Durex Penck Standard, Durex Penck XL
| Applicant | Rb Health (Us), LLC, Parsippany NJ, US |
| Decision | Substantially Equivalent, Nov 6, 2020 |
| Received | Mar 13, 2020 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K200672
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.