510(k) K912134 ยท HRJ Table, Instrument, Powered, Ophthalmic
TBD, LENS MEASURING DEVICE
| Applicant | Alcon Laboratories, Fort Worth TX, US |
| Decision | Substantially Equivalent, Jul 25, 1991 |
| Received | May 14, 1991 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K912134
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.