510(k) K942242 ยท HKO Refractometer, Ophthalmic
AUTO REF-KERATOMETER, RK-3
| Applicant | Cannon U.S.A., Inc., Lake Success NY, US |
| Decision | Substantially Equivalent, Sep 2, 1994 |
| Received | May 9, 1994 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K942242
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.