510(k) K071845 ยท KAM Cannula, Sinus
RELIEVA LUMA SINUS ILLUMINATION SYSTEM, MODEL SIS-100A
| Applicant | Acclarent, Inc., Rmenlo Park CA, US |
| Decision | Substantially Equivalent, Sep 28, 2007 |
| Received | Jul 5, 2007 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K071845
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.