510(k) K092056 ยท HKI Camera, Ophthalmic, Ac-Powered
OPTOMED SMARTSCOPE, MODEL M3-1 EY1
| Applicant | Optomed OY, Oulu, FI |
| Decision | Substantially Equivalent, Oct 1, 2009 |
| Received | Jul 7, 2009 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K092056
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.