510(k) K812097 ยท HNW Dilator, Lachrymal
KOI LACREMAL HOOK & DILATOR
| Applicant | Koi, Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, Aug 18, 1981 |
| Received | Jul 24, 1981 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K812097
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.