510(k) K072302 ยท LRC Instrument, Ent Manual Surgical
ENTELLUS MEDICAL RS-SERIES SYSTEM
| Applicant | Entellus Medical, Inc., Maple Grove MN, US |
| Decision | Substantially Equivalent, Apr 8, 2008 |
| Received | Aug 17, 2007 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K072302
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.