510(k) K913871 ยท DQO Catheter, Intravascular, Diagnostic
FLOSWITCH(R) HP
| Applicant | Boston Scientific Corp, San Jose CA, US |
| Decision | Substantially Equivalent, Nov 25, 1991 |
| Received | Aug 28, 1991 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K913871
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.