510(k) K973273 ยท KAM Cannula, Sinus
XOMED T-STENT, FRONTAL SINUS STENT
| Applicant | Xomed, Inc., Jacksonville FL, US |
| Decision | Substantially Equivalent, Sep 29, 1997 |
| Received | Sep 2, 1997 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K973273
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.