510(k) K013013 ยท DWF Catheter, Cannula And Tubing, Vascular, Cardiopulmonary Bypass
MEDTRONIC DLP ARTERIAL CANNULA WITH 3D TIP - 22 FR.
| Applicant | Medtronic Cardiac Surgical Products, Grand Rapids MI, US |
| Decision | Substantially Equivalent, Dec 4, 2001 |
| Received | Sep 7, 2001 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K013013
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Feb 20, 2014 | Medtronic Inc. Cardiac Rhythm Disease Management Medtronic Select 3D Arterial Cannulae. Vented, model 78622 (22 Fr.). Non-Vented Cannulae, model 78722 (22 Fr.). Sterilized using Ethylene Oxide. Non-pyrogenic.
The Cannula consists of a curved Terminated |
DWF | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.