510(k) K922253 ยท HLQ Keratoscope, Ac-Powered
KERATOREF L60
| Applicant | Luneau Ophtalmologie SA, Chartres Cedex, FR |
| Decision | Substantially Equivalent, Jun 19, 1992 |
| Received | May 1, 1992 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K922253
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.