FDA 510(k) Applications Submitted by Sciton, Inc.

FDA 510(k) Number Submission Date Device Name Applicant
K022466 07/25/2002 PROFILE 1320 LASER SYSTEM SCITON, INC.
K040005 01/02/2004 PROFILE 2000/3000 LASER SYSTEM SCITON, INC.
K060033 01/05/2006 PROFILE MULTI-PLATFORM SYSTEM SCITON, INC.
K070388 02/09/2007 PROFILE MULTI-PLATFORM SYSTEM SCITON, INC.
K081352 05/14/2008 PROFILE MULTI-PLATFORM SYSTEM SCITON, INC.
K111483 05/31/2011 JOULE CLEARSENSE LASER SYSTEM SCITON, INC.
K101916 07/09/2010 JOULE MULTI-PLATFORM SYSTEM SCITON, INC.
K022381 07/22/2002 PROFILE 1320 LASER SYSTEM SCITON, INC.
K032459 08/11/2003 PROFILE 1320 LASER SYSTEM SCITON, INC.
K032460 08/11/2003 PROFILE BBL SYSTEM SCITON, INC.
K122567 08/23/2012 JOULE 810/940/980 MULTI-PLATFORM SYSTEM SCITON, INC.
K023881 11/21/2002 PROFILE 1064 LASER SYSTEM SCITON, INC.
K180508 02/26/2018 JOULE SYSTEM Sciton, Inc.
K002853 09/13/2000 SCITON IMAGE HAIR REMOVAL LASER SCITON, INC.
K003046 09/29/2000 IMAGE VASCULAR LASER SCITON, INC.
K010285 01/31/2001 CONTOUR PROFILE LASER SCITON, INC.
K012552 08/08/2001 SCITON IMAGE HAIR REMOVAL LASER SCITON, INC.


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