510(k) K120988 ยท DWF Catheter, Cannula And Tubing, Vascular, Cardiopulmonary Bypass
DLP SINGLE STAGE VENOUS CANNULA, DLP RIGHT ANGLE SINGLE STAGE VENOUS CANNULA, DLP SINGLE STAGE VENOUS CANNULA WITH RIGHT
| Applicant | Medtronic, Inc., Minneapolis MN, US |
| Decision | Substantially Equivalent, Jul 25, 2012 |
| Received | Apr 2, 2012 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K120988
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Sep 12, 2024 | Medtronic Perfusion Systems Medtronic DLP Single Stage Venous Cannulae with right angle metal tip, REF 67312 Open, Classified |
DWF | None listed |
| Mar 5, 2013 | Medtronic Inc. Cardiac Rhythm Disease Management Medtronic DPL Single Stage Venous Cannula with Metal Tip, used in cardiopulmonary bypass procedures.
Model numbers: 67312; 67314; CB67314; 67316; 67318; CB67318; 67320; 69312; 69314; 69316; 69318 Terminated |
DWF | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.