510(k) K022272 ยท DWF Catheter, Cannula And Tubing, Vascular, Cardiopulmonary Bypass
MALLEABLE SINGLE STAGE VENOUS CANNULA, MODELS 68112-68140 (15 TOTAL CODES)
| Applicant | Medtronic Cardiac Surgical Products, Grad Rapids MI, US |
| Decision | Substantially Equivalent, Jan 8, 2003 |
| Received | Jul 15, 2002 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K022272
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| May 10, 2024 | Medtronic Perfusion Systems Medtronic Venous Cannulae:
a) DLP 20 Fr. Malleable Single Stage Venous Cannula, Model Number 68120,
b) DLP 24 Fr. Malleable Single Stage Venous Cannula, Model Number 68124,
c) DLP 28 Fr. Malleable Open, Classified |
DWF | None listed |
| Jan 18, 2012 | Medtronic Inc. Cardiac Rhythm Disease Management Medtronic, DLP, DLP Malleable Single Stage Venous Cannulae.
Rx Only, Sterilized Using Ethylene Oxide, Nonpyrogenic. Model #'s
68112, 68114, 68116, 68118, 68120, 68122, 68124, 68126, 68128, 68130, 6 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 |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.