510(k) K864225 ยท FAD Stent, Ureteral
ANGIOMED URETERAL D&M SETS/URETEROSCOPY GUID STENT
| Applicant | Angiomed U.S., Inc., Anaheim CA, US |
| Decision | Substantially Equivalent, Jan 30, 1987 |
| Received | Oct 28, 1986 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K864225
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.