K-number	K082494
Device name	DRAD3000E/RADREX-I
Applicant	Toshiba America Medical Systems, In.C
Product code	MQB
Device class	Class II
Decision date	Sep 12, 2008
Decision	Substantially Equivalent
Regulation	892.1680

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View the full FDA submission: accessdata.fda.gov

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DRAD3000E/RADREX-I

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