FDA 510(k) Applications Submitted by BYRON LAMBERT
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K010684 | 03/08/2001 | RX HERCULINK PLUS BILIARY STENT SYSTEM | GUIDANT CORP. |
| K000793 | 03/13/2000 | 1 OTW VIATRAC 18 PERIPHERAL DILATATION CATHETER | GUIDANT CORP. |
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