510(k) K854912 ยท DQX Wire, Guide, Catheter
ANGIOMED GUIED WIRES
| Applicant | Angiomed U.S., Inc., Anaheim CA, US |
| Decision | Substantially Equivalent, Apr 16, 1986 |
| Received | Dec 9, 1985 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K854912
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.