FDA 510(k) Applications Submitted by MATTHEW FOX

FDA 510(k) Number Submission Date Device Name Applicant
K060304 02/06/2006 PHOTEX DIODE LASER SERIES, MODELS 980, 810 AND 940 BIOTEX, INC.
K071328 05/11/2007 VISUALASE THERMAL THERAPY SYSTEM BIOTEX, INC.


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