K-number	K051418
Device name	DIRECT DIGITIZER REGIUS MODEL 370
Applicant	Konica Minolta Medical & Graphic, Inc.
Product code	MQB
Device class	Class II
Decision date	Jul 1, 2005
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 370

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