510(k) K951803 ยท KAM Cannula, Sinus
ROSSITER SINUS STENT
| Applicant | Smith & Nephew Richards, Inc., Bartlett TN, US |
| Decision | Substantially Equivalent, May 11, 1995 |
| Received | Apr 19, 1995 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K951803
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.