FDA 510(k) Applications Submitted by Spectrum Dynamics Medical Ltd

FDA 510(k) Number	Submission Date	Device Name	Applicant
K190457	02/25/2019	VERITON CT whole body SPECT/CT system	Spectrum Dynamics Medical Ltd
K230600	03/03/2023	VERITON CT 300 Series Digital SPECT/CT System (VERITON CT 316/364); VERITON CT 400 Series Digital SPECT/CT System (VERITON CT 416/464)	Spectrum Dynamics Medical Ltd
K161740	06/24/2016	D-SPECT Scanner, D-SPECT L Scanner	Spectrum Dynamics Medical Ltd
K212230	07/16/2021	TruSPECT Radiological Image Processing Station	Spectrum Dynamics Medical Ltd
K182484	09/11/2018	VERITON CT whole body SPECT/CT system	Spectrum Dynamics Medical Ltd