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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