K-number	K093514
Device name	DISCOVERY MODEL NM/CT 670
Applicant	Ge Medical Systems F.I. Haifa
Product code	KPS
Device class	Class II
Decision date	Dec 10, 2009
Decision	Substantially Equivalent
Regulation	892.1200

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Source

View the full FDA submission: accessdata.fda.gov

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DISCOVERY MODEL NM/CT 670

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