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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