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. |
|
|