510(k) K863911 ยท HJK Lens, Contact, Polymethylmethacrylate, Diagnostic
MAINSTER RETINA LASER LENS
| Applicant | Ocular Instruments, Inc., Bellevue WA, US |
| Decision | Substantially Equivalent, Dec 12, 1986 |
| Received | Oct 8, 1986 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K863911
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.