510(k) K924778 ยท HKO Refractometer, Ophthalmic
BURTON AUTO REFRACTOR/KERATOMETER - MODEL BARK-8
| Applicant | R.H. Burton Co., Grove City OH, US |
| Decision | Substantially Equivalent, Apr 5, 1993 |
| Received | Sep 23, 1992 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K924778
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.