510(k) K170520 ยท MLZ Vitrectomy, Instrument Cutter
HyperVit Vitrectomy Probe, 23 GA, HyperVit Vitrectomy Probe, 25+, HyperVit Vitrectomy Probe, 27+
| Applicant | Alcon Research, Ltd., Lake Forest CA, US |
| Decision | Substantially Equivalent, Mar 22, 2017 |
| Received | Feb 22, 2017 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K170520
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.