FDA 510(k) Applications Submitted by RAYMOND T RIDDLE

FDA 510(k) Number Submission Date Device Name Applicant
K060532 02/28/2006 HDR 1000 PLUS WELL CHAMBER, MODEL 90008 STANDARD IMAGING, INC.
K011874 06/15/2001 FADASIS MEDICAL FM-1 NO BLENDER FADASIS MEDICAL, INC.
K001825 06/16/2000 STANDARD IMAGING HDR 1000 PLUS ION CHAMBER; STANDARD IMAGING IVB 1000 ION CHAMBER STANDARD IMAGING, INC.
K002833 09/12/2000 MODIFICATION TO STANDARD IMAGING PT 1000 ION CHAMBER STANDARD IMAGING, INC.
K082773 09/22/2008 STANDARD IMAGING IMSURE BRACHY QA SOFTWARE, MODEL 91331 STANDARD IMAGING, INC.
K042733 10/01/2004 STANDARD IMAGING PIPSPRO QA SOFTWARE SYSTEM STANDARD IMAGING, INC.
K013548 10/24/2001 STANDARD IMAGING IVB 1000 WELL CHAMBER STANDARD IMAGING, INC.
K003665 11/28/2000 FADASSI MEDICAL FM-1 NO BLENDER FADASIS MEDICAL, INC.
K040688 03/16/2004 STANDARD IMAGING E.IMRT CALCULATOR STANDARD IMAGING, INC.
K103193 10/29/2010 DOSEVIEW 3D STANDARD IMAGING, INC.


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