510(k) K854383 ยท HPL Device, Fixation, Ac-Powered, Ophthalmic
KERATOLUX
| Applicant | Carl Zeiss, Inc., Thornwood NY, US |
| Decision | Substantially Equivalent, Nov 12, 1985 |
| Received | Oct 30, 1985 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K854383
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.