510(k) K120962 ยท LRC Instrument, Ent Manual Surgical
PATHASSIST LIGHT FIBER
| Applicant | Entellus Medical, Inc., Maple Grove MN, US |
| Decision | Substantially Equivalent, Apr 27, 2012 |
| Received | Mar 30, 2012 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K120962
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.