510(k) K120917 ยท DQO Catheter, Intravascular, Diagnostic
HEADWAY DUO MICROCATHETER
| Applicant | MicroVention, Inc., Tistin CA, US |
| Decision | Substantially Equivalent, Aug 2, 2012 |
| Received | Mar 27, 2012 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K120917
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.