510(k) K812010 ยท HMX Cannula, Ophthalmic
KOI LACRIMAL INTUBATION SYSTEM
| Applicant | Koi, Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, Jul 28, 1981 |
| Received | Jul 17, 1981 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K812010
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.