510(k) K860332 ยท HNN Knife, Ophthalmic
DIAMOND BLADE MICROMETER KNIFE
| Applicant | Med-Tech Develoment Corp., Clearwater FL, US |
| Decision | Substantially Equivalent, Feb 13, 1986 |
| Received | Jan 29, 1986 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K860332
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.