510(k) K032624 ยท DQO Catheter, Intravascular, Diagnostic
MICRUS MICROCATHETER
| Applicant | Micrus Corp., Sunnyvale CA, US |
| Decision | Substantially Equivalent, Sep 10, 2003 |
| Received | Aug 26, 2003 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K032624
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.