510(k) K093594 ยท KAM Cannula, Sinus
MODIFICATION TO RELIEVA STRATUS MICROFLOW SPACER
| Applicant | Acclarent, Inc., Rmenlo Park CA, US |
| Decision | Substantially Equivalent, Mar 3, 2010 |
| Received | Nov 19, 2009 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K093594
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.