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6F TRIPLE LUMEN POWERLINE CENTRAL VENOUS CATHETER, 5F DUAL LUMEN POWERLINE CENTRAL VENOUS CATHETER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K093927
510(k) Type
Special
Applicant
C.R. BARD, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/4/2010
Days to Decision
44 days
Submission Type
Summary

6F TRIPLE LUMEN POWERLINE CENTRAL VENOUS CATHETER, 5F DUAL LUMEN POWERLINE CENTRAL VENOUS CATHETER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K093927
510(k) Type
Special
Applicant
C.R. BARD, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/4/2010
Days to Decision
44 days
Submission Type
Summary