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FDA 510(k) Applications Submitted by SARABJYOT MANKOO
FDA 510(k) Number
Submission Date
Device Name
Applicant
K093927
12/22/2009
6F TRIPLE LUMEN POWERLINE CENTRAL VENOUS CATHETER, 5F DUAL LUMEN POWERLINE CENTRAL VENOUS CATHETER
C.R. BARD, INC.
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