510(k) K833800 ยท HQC Unit, Phacofragmentation
BEECHER 20 GA. PROBE
| Applicant | Beecher Medical Diagnostic Instrumentation, Mchenry IL, US |
| Decision | Substantially Equivalent, Jan 4, 1984 |
| Received | Oct 31, 1983 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K833800
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.