K-number	K963952
Device name	SERIES 9600 MOBILE DIGITAL IMAGING SYSTEM
Applicant	Ge Dec Medical Systems
Product code	OWB
Device class	Class II
Decision date	Dec 23, 1996
Decision	Substantially Equivalent
Regulation	892.1650

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View the full FDA submission: accessdata.fda.gov

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SERIES 9600 MOBILE DIGITAL IMAGING SYSTEM

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