510(k) K060974 ยท KAM Cannula, Sinus
RELIENT NAVIGATION DEVICE
| Applicant | Acclarent, Inc., Rmenlo Park CA, US |
| Decision | Substantially Equivalent, May 5, 2006 |
| Received | Apr 10, 2006 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K060974
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.