510(k) K845045 ยท DWF Catheter, Cannula And Tubing, Vascular, Cardiopulmonary Bypass
VENOUS RETURN CATHETER SS-1
| Applicant | Dlp, Inc., Grand Rapids MI, US |
| Decision | Substantially Equivalent, Apr 3, 1985 |
| Received | Dec 28, 1984 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K845045
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Jan 18, 2012 | Medtronic Inc. Cardiac Rhythm Disease Management Medtronic DLP, DLP Single Stage Venous Cannulae.
Rx Only, Sterile EO, Nonpyrogenic. Model #'s
66112, 66114, 66116, 66118, 66120, 66122, 66124, 66126, 66128, 66130, 66132, 66134, 66236, 66238, 66240 Terminated |
DWF | None listed |
| Jan 18, 2012 | Medtronic Inc. Cardiac Rhythm Disease Management Medtronic, Single Stage Venous Cannula, Carmeda Bio-Active Surface Venous Cannula, Sterilized Using Ethylene Oxide, Rx Only, Nonpyrogenic.
Model # 's
CB66112, CB66114, CB66116, CB66118, CB66120, C Terminated |
DWF | None listed |
| Sep 29, 2004 | Medtronic Inc Medtronic DLP VAD Venous Cannula for Ventricular Assist, Models 95036 and CB95036. Terminated |
DWF | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.