510(k) K883233 ยท OKS Lacrimal Stents And Intubation Sets
EV MONOCANALICULAR STENT (TM)
| Applicant | Eagle Vision, Inc., Bethesda MD, US |
| Decision | Substantially Equivalent, Aug 22, 1988 |
| Received | Aug 1, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K883233
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.