510(k) K971671 ยท HLI Ophthalmoscope, Ac-Powered
HEIDELBERG RETINA ANGIOGRAPH FA/ICGA (HRA/C)
| Applicant | Heidelberg Engineering, Heidelberg, DE |
| Decision | Substantially Equivalent, Jul 29, 1997 |
| Received | May 7, 1997 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K971671
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.