510(k) K842892 ยท HQL Intraocular Lens
NIDEK DIGITAL KERATOMETER
| Applicant | Nidek, Inc., Walker MI, US |
| Decision | Substantially Equivalent, Oct 5, 1984 |
| Received | Jul 23, 1984 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K842892
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.