K-number	K970063
Device name	SERIES 7600 MOBILE DIGITAL C-ARM
Applicant	Ge Dec Medical Systems
Product code	OWB
Device class	Class II
Decision date	Mar 11, 1997
Decision	Substantially Equivalent
Regulation	892.1650

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View the full FDA submission: accessdata.fda.gov

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SERIES 7600 MOBILE DIGITAL C-ARM

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