510(k) K912366 ยท HJK Lens, Contact, Polymethylmethacrylate, Diagnostic
MAINSTER HIGH MAGNIFICATION LASER LENS
| Applicant | Ocular Instruments, Inc., Bellevue WA, US |
| Decision | Substantially Equivalent, Jun 25, 1991 |
| Received | May 29, 1991 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K912366
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.