510(k) K132440 ยท LRC Instrument, Ent Manual Surgical
XPRESS MULTI-SINUS DILATION TOOL
| Applicant | Entellus Medical, Inc., Plymouth MN, US |
| Decision | Substantially Equivalent, Oct 4, 2013 |
| Received | Aug 6, 2013 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K132440
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.