510(k) K140160 ยท LRC Instrument, Ent Manual Surgical
RELIEVA SCOUT SINUS DILATION SYSTEM
| Applicant | Acclarent, Inc., Rmenlo Park CA, US |
| Decision | Substantially Equivalent, Feb 20, 2014 |
| Received | Jan 22, 2014 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K140160
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.