510(k) K240859 ยท DQX Wire, Guide, Catheter
Glidewire GT-R
| Applicant | Terumo Corporation, Tokyo, JP |
| Decision | Substantially Equivalent, Aug 21, 2024 |
| Received | Mar 28, 2024 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K240859
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.