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DURAMAX CHRONIC HEMODIALYSIS CATHETER AND PROCEDURE KIT

Page Type
Cleared 510(K)
510(k) Number
K101843
510(k) Type
Traditional
Applicant
ANGIODYNAMICS, INC.
Country
United States
FDA Decision
Substantially Equivalent - Kit
Decision Date
10/20/2010
Days to Decision
111 days
Submission Type
Summary

DURAMAX CHRONIC HEMODIALYSIS CATHETER AND PROCEDURE KIT

Page Type
Cleared 510(K)
510(k) Number
K101843
510(k) Type
Traditional
Applicant
ANGIODYNAMICS, INC.
Country
United States
FDA Decision
Substantially Equivalent - Kit
Decision Date
10/20/2010
Days to Decision
111 days
Submission Type
Summary