510(k) K883200 ยท HKO Refractometer, Ophthalmic
CANON AUTOREFRACTOMETER R-22
| Applicant | Canon USA, Inc., Jericho NY, US |
| Decision | Substantially Equivalent, Aug 18, 1988 |
| Received | Jul 28, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K883200
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.