510(k) K111763 ยท LRC Instrument, Ent Manual Surgical
PATHASSIST LIGHT FIBER
| Applicant | Entellus Medical, Inc., Maple Grove MN, US |
| Decision | Substantially Equivalent, Sep 15, 2011 |
| Received | Jun 23, 2011 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K111763
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.