K-number	K182484
Device name	VERITON CT whole body SPECT/CT system
Applicant	Spectrum Dynamics Medical, Ltd.
Product code	KPS
Device class	Class II
Decision date	Nov 9, 2018
Decision	Substantially Equivalent
Regulation	892.1200

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Source

View the full FDA submission: accessdata.fda.gov

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VERITON CT whole body SPECT/CT system

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