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FDA 510(k) Applications Submitted by Sciton, Inc
FDA 510(k) Number
Submission Date
Device Name
Applicant
K213350
10/08/2021
mJOULE System and Accessories
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
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