510(k) K820877 ยท HKO Refractometer, Ophthalmic
AUTOMATIC OBJECTIVE REFRACTOR 2000
| Applicant | Dicon, Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, Jun 25, 1982 |
| Received | Mar 30, 1982 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K820877
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.