510(k) K132297 ยท LRC Instrument, Ent Manual Surgical
EM SINUS DILATION SYSTEM
| Applicant | Medtronic Xomed, Inc., Jacksonville FL, US |
| Decision | Substantially Equivalent, Nov 5, 2013 |
| Received | Jul 24, 2013 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K132297
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.