K-number	K012389
Device name	REVOLUTION XR/D DIGITAL RADIOGRAPHIC IMAGING SYSTEM
Applicant	Ge Medical Systems, Inc.
Product code	KPR
Device class	Class II
Decision date	Aug 10, 2001
Decision	Substantially Equivalent
Regulation	892.1680

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View the full FDA submission: accessdata.fda.gov

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REVOLUTION XR/D DIGITAL RADIOGRAPHIC IMAGING SYSTEM

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