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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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