510(k) K091915 ยท HQC Unit, Phacofragmentation
FLUID ISOLATION DEVICE
| Applicant | Lenstec, Inc., St. Petersburg FL, US |
| Decision | Substantially Equivalent, Oct 27, 2009 |
| Received | Jun 30, 2009 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K091915
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.