K-number	K160933
Device name	Discovery NM 750b Bopsy
Applicant	GE Healthcare
Product code	IYX
Device class	Class I
Decision date	Nov 18, 2016
Decision	Substantially Equivalent
Regulation	892.1100

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Source

View the full FDA submission: accessdata.fda.gov

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Discovery NM 750b Bopsy

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