510(k) K263092 ยท DWF Catheter, Cannula And Tubing, Vascular, Cardiopulmonary Bypass
Dual Stage Venous Cannulae
| Applicant | Sorin Group Italia S.R.L., Mirandola, IT |
| Decision | Substantially Equivalent, Oct 1, 2026 |
| Received | Sep 3, 2026 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K263092
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.