510(k) K890420 ยท DQO Catheter, Intravascular, Diagnostic
USCI 7F GUIDE CATHETER
| Applicant | C.R. Bard, Inc., Billerica MA, US |
| Decision | Substantially Equivalent, Apr 24, 1989 |
| Received | Jan 26, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K890420
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.