510(k) K241158 ยท DQY Catheter, Percutaneous
ASAHI Veloute; ASAHI Veloute C3; ASAHI Tellus; ASAHI Tellus C3
| Applicant | Asahi Intecc Co., Ltd., Seto, JP |
| Decision | Substantially Equivalent, Jun 25, 2024 |
| Received | Apr 26, 2024 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K241158
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.