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FDA 510(k) Applications Submitted by AN NGUYEN
FDA 510(k) Number
Submission Date
Device Name
Applicant
K102709
09/20/2010
PEAK PLASMABLADE PLUS TISSUE DISSECTION DEVICE
PEAK SURGICAL, INC.
K130484
02/25/2013
MAXFORCE BILIARY DILATATION CATHETER AND HURRICANE RX BILIARY CATHETER
BOSTON SCIENTIFIC CORP.
K182244
08/20/2018
Voyant Electrosurgical Generator
Applied Medical Resources Corp.
K172624
09/01/2017
Voyant 5mm Fusion Device
Applied Medical Resources Corporation
K182653
09/25/2018
Voyant Maryland Fusion Device
Applied Medical Resources Corp.
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