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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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