510(k) K110687 ยท KAM Cannula, Sinus
RELIEVA STRATUS PRO MICROFLOW SPACER (FRONTAL)
| Applicant | Acclarent, Inc., Rmenlo Park CA, US |
| Decision | Substantially Equivalent, Oct 7, 2011 |
| Received | Mar 11, 2011 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K110687
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.