510(k) K875353 ยท DWF Catheter, Cannula And Tubing, Vascular, Cardiopulmonary Bypass
PERCUTANEOUS ARTERIAL/VENOUS CANNULA PLACEMENT KIT
| Applicant | Dlp, Inc., Grand Rapids MI, US |
| Decision | Substantially Equivalent, Mar 22, 1988 |
| Received | Dec 31, 1987 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K875353
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Jun 26, 2015 | Medtronic Perfusion Systems Medtronic DLP Femoral Arterial Cannula, models 57414, 57417, and 57421, and DLP Femoral Cannula Replacement Kit, Models 96017 and 96021. Sterilized using Ethylene Oxide.
The cannula and dilator com Terminated |
DWF | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.