510(k) K951179 ยท HKO Refractometer, Ophthalmic
DIGITAL RETINOSCOPIC PHOTOMETER
| Applicant | Kudi Kalu, Inc., Huntsville AL, US |
| Decision | Substantially Equivalent, May 30, 1995 |
| Received | Mar 16, 1995 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K951179
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.