510(k) K061404 ยท OKS Lacrimal Stents And Intubation Sets
MONO-CRAWFORD NASO-LACRIMAL INTUBATION DEVICE
| Applicant | Fci Ophthalmics, Inc., Centercille MA, US |
| Decision | Substantially Equivalent, Aug 7, 2006 |
| Received | May 19, 2006 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K061404
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.