K-number	K083503
Device name	DRAD30003/RADREX-I
Applicant	Toshiba America Medical Systems, In.C
Product code	KPR
Device class	Class II
Decision date	Feb 13, 2009
Decision	Substantially Equivalent
Regulation	892.1680

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View the full FDA submission: accessdata.fda.gov

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DRAD30003/RADREX-I

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