510(k) K830379 ยท HQC Unit, Phacofragmentation
PHAKO KIT
| Applicant | Vxtra Corp., Mchenry IL, US |
| Decision | Substantially Equivalent, Apr 5, 1983 |
| Received | Feb 4, 1983 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K830379
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.