510(k) K895180 ยท DQO Catheter, Intravascular, Diagnostic
USCI 7F LARGE LUMEN GUIDING CATHETER
| Applicant | C.R. Bard, Inc., Billerica MA, US |
| Decision | Substantially Equivalent, Apr 23, 1990 |
| Received | Aug 10, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K895180
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.