510(k) K102003 ยท LRC Instrument, Ent Manual Surgical
XPRESS BALLOON DEVICE
| Applicant | Entellus Medical, Inc., Maple Grove MN, US |
| Decision | Substantially Equivalent, Oct 22, 2010 |
| Received | Jul 15, 2010 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K102003
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.