510(k) K213315 ยท DQX Wire, Guide, Catheter
CROSSLEAD Peripheral Guide Wire
| Applicant | Asahi Intecc Co., Ltd., Seto, JP |
| Decision | Substantially Equivalent, Jul 1, 2022 |
| Received | Oct 4, 2021 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K213315
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.