510(k) K854487 ยท DWF Catheter, Cannula And Tubing, Vascular, Cardiopulmonary Bypass
VENOUS RETURN CANNULA W/CUFF 91039
| Applicant | Dlp, Inc., Grand Rapids MI, US |
| Decision | Substantially Equivalent, Feb 10, 1986 |
| Received | Nov 8, 1985 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K854487
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Jan 18, 2012 | Medtronic Inc. Cardiac Rhythm Disease Management Medtronic, DLP, DLP Malleable Single Stage Venous CannulaeRx Only, Sterilized Using Ethylene Oxide, Nonpyrogenic.
Model # 91037.
These cannulae are intended for collection of venous blood from the Terminated |
DWF | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.