FDA 510(k) Applications Submitted by KOBBY DANKWAH
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K000101 | 01/13/2000 | RX VIATRAC 14 PERIPHERAL DILATATION CATHETER | GUIDANT CORP. |
| K991032 | 03/29/1999 | GUIDANT MEGALINK BILIARY STENT, MODEL FG1002949-58 | GUIDANT CORP. |
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