K-number	K951765
Device name	SERIES 6600 DIGITAL MOBILE C-ARM
Applicant	Ge Dec Medical Systems
Product code	OXO
Device class	Class II
Decision date	May 11, 1995
Decision	Substantially Equivalent
Regulation	892.1650

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View the full FDA submission: accessdata.fda.gov

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SERIES 6600 DIGITAL MOBILE C-ARM

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