FDA 510(k) Applications Submitted by Novarad Corporation

FDA 510(k) Number Submission Date Device Name Applicant
K220146 01/19/2022 VisAR Novarad Corporation
K160371 02/10/2016 NovaPACS NOVARAD CORPORATION
K171754 06/13/2017 NovaPACS Novarad Corporation
K172418 08/10/2017 OpenSight Novarad Corporation


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