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MULTI-LUMEN CENTRAL VENOUS CATHETER SET

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K904404
510(k) Type
Traditional
Applicant
ARROW INTL., INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/15/1991
Days to Decision
143 days

MULTI-LUMEN CENTRAL VENOUS CATHETER SET

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K904404
510(k) Type
Traditional
Applicant
ARROW INTL., INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/15/1991
Days to Decision
143 days