510(k) K262052 ยท DWF Catheter, Cannula And Tubing, Vascular, Cardiopulmonary Bypass
Tri Stage Venous Cannulae
| Applicant | Sorin Group Italia S.R.L., Mirandola, IT |
| Decision | Substantially Equivalent, Sep 28, 2026 |
| Received | Jun 18, 2026 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K262052
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.