FDA 510(k) Applications Submitted by BRADY ALLER

FDA 510(k) Number Submission Date Device Name Applicant
K090250 02/02/2009 ELECTRO-LIGHT THERAPY HILL LABORATORIES CO.
K072256 08/13/2007 HF54 COMBINATION ULTRASOUND INTERFERENTIAL AND PREMODULATED STIMULATION SYSTEM WITH OPTIONAL HANDS-FREE OPERATION, MODEL HILL LABORATORIES CO.
K063034 10/03/2006 AIR-FLEX WITH AUTO-DISTRACTION HILL LABORATORIES CO.
K083183 10/28/2008 AKLARUS PHOTOTHERAPY SYSTEM HILL LABORATORIES CO.


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