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NEXTSTEP ANTEGRADE CHRONIC HEMODIALYSIS CATHETER

Page Type
Cleared 510(K)
510(k) Number
K111900
510(k) Type
Traditional
Applicant
Teleflex Medical, Inc.
Country
United States
FDA Decision
Substantially Equivalent - Kit
Decision Date
8/17/2011
Days to Decision
43 days
Submission Type
Summary

NEXTSTEP ANTEGRADE CHRONIC HEMODIALYSIS CATHETER

Page Type
Cleared 510(K)
510(k) Number
K111900
510(k) Type
Traditional
Applicant
Teleflex Medical, Inc.
Country
United States
FDA Decision
Substantially Equivalent - Kit
Decision Date
8/17/2011
Days to Decision
43 days
Submission Type
Summary