510(k) K972252 ยท HQC Unit, Phacofragmentation
VISTA UNIVERSAL HANDPIECE
| Applicant | Odyssey Technologies, Inc., Temple City CA, US |
| Decision | Substantially Equivalent, Jul 29, 1997 |
| Received | Jun 16, 1997 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K972252
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.