510(k) K110739 ยท LRC Instrument, Ent Manual Surgical
ENTELLUS MEDICAL SINUS GUIDEWIRE
| Applicant | Entellus Medical, Inc., Maple Grove MN, US |
| Decision | Substantially Equivalent, Jun 14, 2011 |
| Received | Mar 17, 2011 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K110739
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.