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TWO-LUMEN CENTRAL VENOUS ACCESS KIT WITH HEMOSTASIS VALVE/SIDE PORT

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K002507
510(k) Type
Traditional
Applicant
Arrow Intl., Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/21/2001
Days to Decision
218 days
Submission Type
Summary

TWO-LUMEN CENTRAL VENOUS ACCESS KIT WITH HEMOSTASIS VALVE/SIDE PORT

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K002507
510(k) Type
Traditional
Applicant
Arrow Intl., Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/21/2001
Days to Decision
218 days
Submission Type
Summary