510(k) K142252 ยท LRC Instrument, Ent Manual Surgical
XprESS Multi-Sinus Dilation Tool
| Applicant | Entellus Medical, Inc., Plymouth MN, US |
| Decision | Substantially Equivalent, Oct 17, 2014 |
| Received | Aug 14, 2014 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K142252
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.