510(k) K944261 ยท HLI Ophthalmoscope, Ac-Powered
RETINA ANGIOGRAPH
| Applicant | Heidelberg Engineering, D06900 Heidelberg,Germany, DE |
| Decision | Substantially Equivalent, Nov 14, 1994 |
| Received | Sep 1, 1994 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K944261
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.