510(k) K974479 ยท KXP Stent, Vaginal
SILIMED VAGINAL STENT
| Applicant | Silimed, LLC, Crofton MD, US |
| Decision | Substantially Equivalent, Aug 5, 1998 |
| Received | Nov 26, 1997 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K974479
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.