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Arrow Pressure Injectable Midline Catheter

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K213855
510(k) Type
Traditional
Applicant
Arrow International LLC Subsidiary of Teleflex Incorporated
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/2/2022
Days to Decision
266 days
Submission Type
Summary

Arrow Pressure Injectable Midline Catheter

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K213855
510(k) Type
Traditional
Applicant
Arrow International LLC Subsidiary of Teleflex Incorporated
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/2/2022
Days to Decision
266 days
Submission Type
Summary