510(k) K935233 ยท OKS Lacrimal Stents And Intubation Sets
IOLAB LACRIMAL DUCT CATHETER
| Applicant | Chiron Vision Corp., Irvine CA, US |
| Decision | Substantially Equivalent, Sep 15, 1994 |
| Received | Nov 1, 1993 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K935233
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.