510(k) K241962 ยท DQX Wire, Guide, Catheter
Crossloop
| Applicant | Asahi Intecc Co., Ltd., Seto, JP |
| Decision | Substantially Equivalent, Mar 27, 2025 |
| Received | Jul 3, 2024 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K241962
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.