510(k) K855140 ยท KOD Catheter, Urological
ANGIOMED RENAL DILATION SET
| Applicant | Angiomed U.S., Inc., Anaheim CA, US |
| Decision | Substantially Equivalent, Feb 24, 1986 |
| Received | Dec 26, 1985 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K855140
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.