510(k) K925757 ยท HLJ Ophthalmoscope, Battery-Powered
OPHTHALMOSCOPE
| Applicant | Rudolf Riester GmbH & Co. KG, D-72417 Jungingen, DE |
| Decision | Substantially Equivalent, Aug 3, 1993 |
| Received | Nov 13, 1992 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K925757
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.