510(k) K012096 ยท HJK Lens, Contact, Polymethylmethacrylate, Diagnostic
DISPOSABLE VITRECTOMY LENS
| Applicant | Ocular Instruments, Inc., Bellevue WA, US |
| Decision | Substantially Equivalent, Aug 24, 2001 |
| Received | Jul 5, 2001 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K012096
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.