510(k) K830366 ยท HNN Knife, Ophthalmic
DIAMOND KNIFE
| Applicant | Koi, Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, Mar 9, 1983 |
| Received | Feb 4, 1983 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K830366
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.