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Arrow Quickflash Arterial Catheterization Device

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K160018
510(k) Type
Traditional
Applicant
Arrow International, Inc. (Subsidiary of Teleflex, Inc.)
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/13/2016
Days to Decision
160 days
Submission Type
Summary

Arrow Quickflash Arterial Catheterization Device

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K160018
510(k) Type
Traditional
Applicant
Arrow International, Inc. (Subsidiary of Teleflex, Inc.)
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/13/2016
Days to Decision
160 days
Submission Type
Summary