510(k) K884502 ยท DQO Catheter, Intravascular, Diagnostic
USCI 8F EXTRA LARGE LUMEN GUIDE CATHETER
| Applicant | C.R. Bard, Inc., Billerica MA, US |
| Decision | Substantially Equivalent, Jan 18, 1989 |
| Received | Oct 26, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K884502
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.