510(k) K830770 ยท HLX Photostimulator, Ac-Powered
CONTRAST SENSITIVITY EQUIPMENT
| Applicant | Cadwell Laboratories, Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, Apr 28, 1983 |
| Received | Mar 11, 1983 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K830770
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.