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

PEDIATRIC AORTIC ROOT CANNULA

K Number: K040173 · Decision Mar 19, 2004
Classifications
1
FEI Numbers
108
Registration Numbers
108
Same Product Code
393
Applicant Total
28
Review Days
53

Basic Information

Device Name
PEDIATRIC AORTIC ROOT CANNULA
K Number
K040173
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
870.4210
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
MEDTRONIC PERFUSION SYSTEMS
Date Received
January 26, 2004
Decision Date
March 19, 2004
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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