510(k) K141916 ยท LRC Instrument, Ent Manual Surgical
PATHASSIST LED LIGHT FIBER
| Applicant | Entellus Medical, Inc., Plymouth MN, US |
| Decision | Substantially Equivalent, Aug 7, 2014 |
| Received | Jul 15, 2014 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K141916
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.