510(k) K781313 ยท HPL Device, Fixation, Ac-Powered, Ophthalmic
VISION-STIMULATOR, CAM
| Applicant | Clement Clarke, Inc. MD, US |
| Decision | Substantially Equivalent, Jan 26, 1979 |
| Received | Jul 31, 1978 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K781313
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.