510(k) K150232 ยท DQO Catheter, Intravascular, Diagnostic
Radifocus Optitorque Angiographic Catheter
| Applicant | Ashitaka Factory of Terumo Corp., Fujinomiya Shizuoka, JP |
| Decision | Substantially Equivalent, Oct 19, 2015 |
| Received | Feb 2, 2015 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K150232
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.