K-number	K173816
Device name	NM/CT 850, NM/CT 860
Applicant	GE Healthcare
Product code	KPS
Device class	Class II
Decision date	Apr 17, 2018
Decision	Substantially Equivalent
Regulation	892.1200

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Source

View the full FDA submission: accessdata.fda.gov

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NM/CT 850, NM/CT 860

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