510(k) K130503 ยท LRC Instrument, Ent Manual Surgical
PATHASSIST LED LIGHT FIBER
| Applicant | Entellus Medical, Inc., Plymouth MN, US |
| Decision | Substantially Equivalent, Jun 11, 2013 |
| Received | Feb 27, 2013 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K130503
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.