510(k) K991238 ยท OKS Lacrimal Stents And Intubation Sets
FCI CRAWFORD PROBE INTUBATION SETS
| Applicant | Fci Ophthalmics, Inc., Marshfield Hills MA, US |
| Decision | Substantially Equivalent, Jul 8, 1999 |
| Received | Apr 12, 1999 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K991238
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.