510(k) K925304 ยท HKO Refractometer, Ophthalmic
AUTOREF LENSMETER RL-10
| Applicant | Canon USA, Inc., Tokyo 146, JP |
| Decision | Substantially Equivalent, Feb 17, 1994 |
| Received | Oct 21, 1992 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K925304
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.