510(k) K152121 ยท LRC Instrument, Ent Manual Surgical
NuVent EM Sinus Dilation System
| Applicant | Medtronic Xomed, Inc., Jacksonville FL, US |
| Decision | Substantially Equivalent, Dec 1, 2015 |
| Received | Jul 30, 2015 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K152121
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.