FDA 510(k) Applications Submitted by Jay M/ Patel

FDA 510(k) Number Submission Date Device Name Applicant
K213350 10/08/2021 mJOULE System and Accessories 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.
K213761 12/01/2021 Joule diVa System Sciton, Inc
K182173 08/10/2018 Joule System Sciton, Inc
K173285 10/16/2017 JOULE SYSTEM Sciton, Inc
K180508 02/26/2018 JOULE SYSTEM Sciton, Inc.
K071610 06/13/2007 MEDIAID PULSE OXIMETER M30 AND M34 MEDIAID INC.
K071642 06/18/2007 MEDIAID M960 SERIES, VITAL SIGNS MONITOR AND MEDIAID M900 SERIES, PULSE OXIMETER MEDIAID INC.


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