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DUET LONG-TERM HEMODIALYSIS CATHETER SYSTEM, DUET LONG-TERM HEMODIALYSIS CATHETER SYSTEM CATHETER REPAIR KIT

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K090528
510(k) Type
Traditional
Applicant
C.R. Bard, Inc.
Country
United States
FDA Decision
Substantially Equivalent - Kit
Decision Date
5/28/2009
Days to Decision
90 days
Submission Type
Summary

DUET LONG-TERM HEMODIALYSIS CATHETER SYSTEM, DUET LONG-TERM HEMODIALYSIS CATHETER SYSTEM CATHETER REPAIR KIT

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K090528
510(k) Type
Traditional
Applicant
C.R. Bard, Inc.
Country
United States
FDA Decision
Substantially Equivalent - Kit
Decision Date
5/28/2009
Days to Decision
90 days
Submission Type
Summary