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DURAFLOW 2 CHRONIC HEMODIALYSIS CATHETER AND PROCEDURE KIT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K110936
510(k) Type
Traditional
Applicant
ANGIODYNAMICS, INC.
Country
United States
FDA Decision
Substantially Equivalent - Kit
Decision Date
6/10/2011
Days to Decision
67 days
Submission Type
Summary

DURAFLOW 2 CHRONIC HEMODIALYSIS CATHETER AND PROCEDURE KIT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K110936
510(k) Type
Traditional
Applicant
ANGIODYNAMICS, INC.
Country
United States
FDA Decision
Substantially Equivalent - Kit
Decision Date
6/10/2011
Days to Decision
67 days
Submission Type
Summary