510(k) K152740 ยท DQX Wire, Guide, Catheter
Radifocus Glidewire
| Applicant | Ashitaka Factory of Terumo Corp., Fujinomiya Shizuoka, JP |
| Decision | Substantially Equivalent, Nov 16, 2015 |
| Received | Sep 23, 2015 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K152740
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.