510(k) K854054 ยท HLR Keratoscope, Battery-Powered
PLACIDO DISC
| Applicant | Cutler Medical Instruments, Santa Monica CA, US |
| Decision | Substantially Equivalent, Dec 27, 1985 |
| Received | Oct 3, 1985 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K854054
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.