510(k) K243757 ยท DQY Catheter, Percutaneous
Shockwave CS Guide Catheter
| Applicant | Shockwave Medical, Inc., Santa Clara CA, US |
| Decision | Substantially Equivalent, May 2, 2025 |
| Received | Dec 6, 2024 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K243757
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.