510(k) K170417 ยท DQX Wire, Guide, Catheter
Glidewire GT
| Applicant | Terumo Corporation, Shibuya-Ku, JP |
| Decision | Substantially Equivalent, Sep 15, 2017 |
| Received | Feb 10, 2017 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K170417
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.