510(k) K170247 ยท OKS Lacrimal Stents And Intubation Sets
Lacriflow CL
| Applicant | Kaneka Pharma America, LLC, New York NY, US |
| Decision | Substantially Equivalent, Apr 18, 2017 |
| Received | Jan 27, 2017 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K170247
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.