510(k) K895542 ยท DQO Catheter, Intravascular, Diagnostic
SONICATH(TM) 5 F
| Applicant | Boston Scientific Corp, Watertown MA, US |
| Decision | Substantially Equivalent, Apr 6, 1990 |
| Received | Sep 13, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K895542
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.