510(k) K896198 ยท HJK Lens, Contact, Polymethylmethacrylate, Diagnostic
MAINSTER WIDE FIELD LASER LENS
| Applicant | Ocular Instruments, Inc., Bellevue WA, US |
| Decision | Substantially Equivalent, Dec 18, 1989 |
| Received | Oct 27, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K896198
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.