FDA 510(k) Applications Submitted by SUN NUCLEAR CORPORATION

FDA 510(k) Number Submission Date Device Name Applicant
K160057 01/12/2016 ArcCHECK-MR Sun Nuclear Corporation
K150848 03/31/2015 Dose Calculator SUN NUCLEAR CORPORATION
K142142 08/05/2014 QUALITY REPORTS SUN NUCLEAR CORPORATION
K131466 05/21/2013 MAPCHECK2, ARCCHECK SUN NUCLEAR CORPORATION
K131704 06/11/2013 EPIDOSE SUN NUCLEAR CORPORATION
K131862 06/24/2013 3DVH SUN NUCLEAR CORPORATION
K141800 07/03/2014 PERFRACTION SUN NUCLEAR CORPORATION
K142431 08/29/2014 WaterProof PROFILER SUN NUCLEAR CORPORATION
K142617 09/16/2014 ArcCHECK SUN NUCLEAR CORPORATION
K170307 02/01/2017 SunCHECK SUN NUCLEAR CORPORATION
K161946 07/15/2016 DoseCHECK Sun Nuclear Corporation


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