510(k) K111875 ยท LRC Instrument, Ent Manual Surgical
RELIEVA SPIN SINUS DILATION SYSTEM
| Applicant | Acclarent, Inc., Rmenlo Park CA, US |
| Decision | Substantially Equivalent, Oct 11, 2011 |
| Received | Jul 1, 2011 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K111875
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.