510(k) K800112 ยท HPL Device, Fixation, Ac-Powered, Ophthalmic
AMBLYOPIA TRAINER
| Applicant | Life-Tech Instruments, Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, Mar 10, 1980 |
| Received | Jan 16, 1980 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K800112
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.