510(k) K093305 ยท MLZ Vitrectomy, Instrument Cutter
ENHANCED ULTRA VIT PROBE
| Applicant | Alcon Research, Ltd., Irvine CA, US |
| Decision | Substantially Equivalent, Apr 2, 2010 |
| Received | Oct 22, 2009 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K093305
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.