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FDA 510(k) Applications Submitted by PETER N 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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