510(k) K854910 ยท DQO Catheter, Intravascular, Diagnostic
ANGIOFLOW
| Applicant | Angiomed U.S., Inc., Anaheim CA, US |
| Decision | Substantially Equivalent, Jul 17, 1986 |
| Received | Dec 9, 1985 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K854910
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.