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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