ClearanceBrief
510(k) K842375 ยท DWF Catheter, Cannula And Tubing, Vascular, Cardiopulmonary Bypass

VENOUS CANNULA W/BENT, TIP WIRE

ApplicantDlp, Inc., Mchenry IL, US
DecisionSubstantially Equivalent, Aug 10, 1984
ReceivedJun 18, 1984
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K842375

DateFirm and productCodeLinked 510(k)
Mar 5, 2013Medtronic Inc. Cardiac Rhythm Disease Management
Medtronic DPL Single Stage Venous Cannula with Metal Tip, used in cardiopulmonary bypass procedures. Model numbers: 67312; 67314; CB67314; 67316; 67318; CB67318; 67320; 69312; 69314; 69316; 69318
Terminated
DWFNone listed
Jan 18, 2012Medtronic Inc. Cardiac Rhythm Disease Management
Medtronic DLP, DLP Single Stage Venous Cannula w/Right Angle Metal Tip. Rx Only, Sterile EO, Nonpyrogenic. Model number #'s : 67312, 67314, 67316, 67318, 67320, 69312, 69314, 69316, 69318, 68320,
Terminated
DWFNone listed
Jan 18, 2012Medtronic Inc. Cardiac Rhythm Disease Management
Medtronic, DLP, DLP Right Angle Single Stage Venous Cannulae. Rx Only, Sterile EO, Nonpyrogenic. Model #'s 67512, 67514, 67516, 67518, 67520, 67522, 67524, 67526, 67528, 67530, 67532, 67534, 67636.
Terminated
DWFNone listed
Jan 18, 2012Medtronic 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
DWFNone listed
Jul 24, 2008Medtronic Perfusion Systems
Medtronic Venous Cannula with bent tip wire, for vascular cardiopulmonary bypass. Catalog Number: CB67532
Terminated
DWFNone listed

Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.