510(k) K914393 ยท HLX Photostimulator, Ac-Powered
RETINA TESTER
| Applicant | Retina Tester, Memphis TN, US |
| Decision | Substantially Equivalent, Mar 2, 1992 |
| Received | Oct 1, 1991 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K914393
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.