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FDA 510(k) Applications Submitted by Greg Wiita
FDA 510(k) Number
Submission Date
Device Name
Applicant
K030518
02/19/2003
AMERITEK SURE-POINT TRACKER SYSTEM
AMERTEK MEDICAL, INC.
K031273
04/22/2003
AMERITEK SURE-POINT HDR NEEDLE TEMPLATE
AMERTEK MEDICAL, INC.
K011581
05/23/2001
AMERITEK BRACHYTHERAPY TEMPLATE
AMERTEK MEDICAL, INC.
K972152
06/09/1997
DEVMED STEPPING AND STABILIZING SYSTEM
DEVMED CORP.
K173533
11/15/2017
Duette 100% Silicone Dual-Balloon, Temperature-Sensing Catheter
Poiesis Medical, LLC
K024183
12/19/2002
ALTON PT STEPPER
ALTON DESIGN, LLC
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