K-number	K210880
Device name	Vereos PET/CT
Applicant	Philips Medical Systems Nederland B.V.
Product code	KPS
Device class	Class II
Decision date	May 19, 2021
Decision	Substantially Equivalent
Regulation	892.1200

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Source

View the full FDA submission: accessdata.fda.gov

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Vereos PET/CT

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