510(k) K131939 ยท HLI Ophthalmoscope, Ac-Powered
AMICO DH-W35 OPHTHALMOSCOPE SERIES
| Applicant | Amico Diagnostic Incorporated, Apollo Beach FL, US |
| Decision | Substantially Equivalent, Mar 26, 2014 |
| Received | Jun 27, 2013 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K131939
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.