510(k) K230377 ยท DQX Wire, Guide, Catheter
CROSSLEAD Penetration Peripheral Guide Wire
| Applicant | Asahi Intecc Co., Ltd., Seto, JP |
| Decision | Substantially Equivalent, Jul 20, 2023 |
| Received | Feb 13, 2023 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K230377
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.