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MULTILUMEN CENTRAL VENOUS CATH. W/VITACUFF DEVICE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K882448
510(k) Type
Traditional
Applicant
BD BECTON DICKINSON VACUTAINER SYSTEMS PREANALYTIC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/9/1988
Days to Decision
56 days

MULTILUMEN CENTRAL VENOUS CATH. W/VITACUFF DEVICE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K882448
510(k) Type
Traditional
Applicant
BD BECTON DICKINSON VACUTAINER SYSTEMS PREANALYTIC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/9/1988
Days to Decision
56 days