FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

MC2 TWO-STAGE VENOUS CANNULA, OVAL MC2 TWO-STAGE VENOUS CANNULA, THIN WALL TWO-STAGE VENOUS CANNULA, MC2X THREE-STAGE VE

K Number: K140165 · Decision May 20, 2014
Classifications
1
FEI Numbers
108
Registration Numbers
108
Same Product Code
393
Applicant Total
25
Review Days
118

Basic Information

Device Name
MC2 TWO-STAGE VENOUS CANNULA, OVAL MC2 TWO-STAGE VENOUS CANNULA, THIN WALL TWO-STAGE VENOUS CANNULA, MC2X THREE-STAGE VE
K Number
K140165
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.4210
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
MEDTRONIC, INC.
Date Received
January 22, 2014
Decision Date
May 20, 2014
Product Code
DWF
Advisory Committee
Cardiovascular
Review Advisory Committee
CV
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
DWF Catheter, Cannula And Tubing, Vascular, Cardiopulmonary Bypass

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