510(k) K180456 ยท DWF Catheter, Cannula And Tubing, Vascular, Cardiopulmonary Bypass
Bio-Medicus Adult Cannulae Kit
| Applicant | Medtronic, Inc., Mounds View MN, US |
| Decision | Substantially Equivalent, Mar 22, 2018 |
| Received | Feb 20, 2018 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K180456
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Jul 15, 2026 | Medtronic Perfusion Systems Medtronic DLP One-Piece Pediatric Arterial Cannula, Product Number/CFN 77010; Cardiopulmonary bypass vascular cannula Open, Classified |
DWF | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.