510(k) K782141 ยท HQC Unit, Phacofragmentation
LEVIGATOR, KEELER PHOKO
| Applicant | Keeler Optical Products , Ltd., Mchenry IL, US |
| Decision | Substantially Equivalent, Jan 26, 1979 |
| Received | Dec 27, 1978 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K782141
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.