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Multi-Lumen Acute Hemodialysis Catheter for High Volume Infusions

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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