K-number	K092717
Device name	DIRECT DIGITIZER, REGIUS MODEL 210
Applicant	Konica Minolta Medical & Graphic, Inc.
Product code	MQB
Device class	Class II
Decision date	Oct 30, 2009
Decision	Substantially Equivalent
Regulation	892.1680

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View the full FDA submission: accessdata.fda.gov

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DIRECT DIGITIZER, REGIUS MODEL 210

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