510(k) K073041 ยท KAM Cannula, Sinus
RELIEVA AND RELIEVA ACELLA SINUS BALLOON CATHETER
| Applicant | Acclarent, Inc., Rmenlo Park CA, US |
| Decision | Substantially Equivalent, Mar 11, 2008 |
| Received | Oct 29, 2007 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K073041
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.