510(k) K904788 ยท DQO Catheter, Intravascular, Diagnostic
MEWISSEN CATHETER
| Applicant | Boston Scientific Corp, San Jose CA, US |
| Decision | Substantially Equivalent, Dec 17, 1990 |
| Received | Oct 23, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K904788
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.