510(k) K943955 ยท HLI Ophthalmoscope, Ac-Powered
RETINA FLOWMETER
| Applicant | Heidelberg Engineering, D06900 Heidelberg,Germany, DE |
| Decision | Substantially Equivalent, Nov 14, 1994 |
| Received | Aug 15, 1994 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K943955
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.