510(k) K201892 · OKS Lacrimal Stents And Intubation Sets
Ritleng®+ and Ritleng®+ PVP
| Applicant | Fci (France Chirurgie Instrumentation) Sas, Paris, FR |
| Decision | Substantially Equivalent, Mar 11, 2021 |
| Received | Jul 8, 2020 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K201892
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.