FDA 510(k) Applications Submitted by PROWESS, INC.

FDA 510(k) Number Submission Date Device Name Applicant
K100801 03/22/2010 PUMA MODEL VERSION 1.0 PROWESS, INC.
K101076 04/19/2010 PROWESS PANTHER PROARC, MODEL VERSION 5.0 PROWESS, INC.
K122616 08/27/2012 PANTHER OIS/R & V MODEL VERSION 2.0 PROWESS, INC.
K083502 11/25/2008 PANTHER REALART, MODEL 4.7 PROWESS, INC.
K143514 12/11/2014 Panther StereoSeed PROWESS, INC.
K032456 08/11/2003 PROWESS PROWESS, INC.


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