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

ONE PIECE PEDIATRIC ARTERIAL CANNULA, MODEL: 77006, 77106

K Number: K024069 · Decision Jan 8, 2003
Classifications
1
FEI Numbers
108
Registration Numbers
108
Same Product Code
393
Applicant Total
468
Review Days
29

Basic Information

Device Name
ONE PIECE PEDIATRIC ARTERIAL CANNULA, MODEL: 77006, 77106
K Number
K024069
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
870.4210
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
MEDTRONIC VASCULAR
Date Received
December 10, 2002
Decision Date
January 8, 2003
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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