FDA 510(k) Applications Submitted by PETER ALLEN

FDA 510(k) Number Submission Date Device Name Applicant
K070466 02/16/2007 REVOLIX DUO LASER SYSTEM ALLMED SYSTEMS INC.
K070476 02/20/2007 REVOLIX 120 ALLMED SYSTEMS INC.
K070924 04/03/2007 FLEXGUARD ALLMED SYSTEMS INC.
K110941 04/04/2011 REVOLIX JR 30, REVOLIX JR 50, REVOLIX JR 160, REVOLIX FR 200 ALLMED SYSTEMS INC.
K002853 09/13/2000 SCITON IMAGE HAIR REMOVAL LASER SCITON, INC.
K132975 09/23/2013 SPHINX JR ALLMED SYSTEMS INC.
K003046 09/29/2000 IMAGE VASCULAR LASER SCITON, INC.
K033423 10/27/2003 REVOLIX LASER SYSTEMS ALLMED SYSTEMS INC.
K033437 10/28/2003 SPHINX LASER SYSTEMS ALLMED SYSTEMS INC.
K010285 01/31/2001 CONTOUR PROFILE LASER SCITON, INC.
K051167 05/05/2005 REVOLIX AND REVOLIX JR ALLMED SYSTEMS INC.
K012552 08/08/2001 SCITON IMAGE HAIR REMOVAL LASER SCITON, INC.


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