510(k) K980575 ยท DQO Catheter, Intravascular, Diagnostic
SITESEER ANGIOGRAPHIC CATHETER
| Applicant | C.R. Bard, Inc., Billerica MA, US |
| Decision | Substantially Equivalent, May 15, 1998 |
| Received | Feb 17, 1998 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K980575
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.