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Multi-Lumen Acute Hemodialysis Catheter for High Volume Infusions

Page Type
Cleared 510(K)
510(k) Number
K143102
510(k) Type
Traditional
Applicant
Arrow International, Inc. (Subsidiary OF Teleflex, Inc.)
Country
United States
FDA Decision
Substantially Equivalent - Kit with Drugs
Decision Date
7/24/2015
Days to Decision
268 days
Submission Type
Summary

Multi-Lumen Acute Hemodialysis Catheter for High Volume Infusions

Page Type
Cleared 510(K)
510(k) Number
K143102
510(k) Type
Traditional
Applicant
Arrow International, Inc. (Subsidiary OF Teleflex, Inc.)
Country
United States
FDA Decision
Substantially Equivalent - Kit with Drugs
Decision Date
7/24/2015
Days to Decision
268 days
Submission Type
Summary