510(k) K081542 ยท LRC Instrument, Ent Manual Surgical
MODIFICATION TO ENTELLUS MEDICAL RS-SERIES SYSTEM
| Applicant | Entellus Medical, Inc., Plymouth MN, US |
| Decision | Substantially Equivalent, Jun 27, 2008 |
| Received | Jun 2, 2008 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K081542
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.