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ANTIMICROBIAL MULTI-LUMEN CENTRAL VENOUS CATHETER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K900263
510(k) Type
Traditional
Applicant
ARROW INTL., INC.
Country
United States
FDA Decision
Substantially Equivalent - Kit
Decision Date
7/24/1990
Days to Decision
187 days

ANTIMICROBIAL MULTI-LUMEN CENTRAL VENOUS CATHETER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K900263
510(k) Type
Traditional
Applicant
ARROW INTL., INC.
Country
United States
FDA Decision
Substantially Equivalent - Kit
Decision Date
7/24/1990
Days to Decision
187 days