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

AngioVac Cannula

K Number: K253106 · Decision Oct 24, 2025
Classifications
1
FEI Numbers
104
Registration Numbers
104
Same Product Code
400
Applicant Total
87
Review Days
30

Basic Information

Device Name
AngioVac Cannula
K Number
K253106
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
870.4210
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
AngioDynamics, Inc.
Date Received
September 24, 2025
Decision Date
October 24, 2025
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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