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ANGIODYNAMICS, INC., DURAMAX HEMODIALYSIS CATHETER AND PROCEDURE KIT

Page Type
Cleared 510(K)
510(k) Number
K080400
510(k) Type
Traditional
Applicant
ANGIODYNAMICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/13/2008
Days to Decision
90 days
Submission Type
Summary

ANGIODYNAMICS, INC., DURAMAX HEMODIALYSIS CATHETER AND PROCEDURE KIT

Page Type
Cleared 510(K)
510(k) Number
K080400
510(k) Type
Traditional
Applicant
ANGIODYNAMICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/13/2008
Days to Decision
90 days
Submission Type
Summary