510(k) K760199 ยท HLZ Electrode, Corneal
ELECTRORETINOGRAPH
| Applicant | Lkc Technologies, Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, Aug 4, 1976 |
| Received | Jul 7, 1976 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K760199
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.