510(k) K252295 ยท LOX Catheters, Transluminal Coronary Angioplasty, Percutaneous
Ryurei
| Applicant | Terumo Corporation, Tokyo, JP |
| Decision | Substantially Equivalent, Mar 27, 2026 |
| Received | Jul 23, 2025 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K252295
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.