K-number	K083649
Device name	CARDIUS 3 X-ACT
Applicant	Digirad Corp.
Product code	KPS
Device class	Class II
Decision date	Mar 9, 2009
Decision	Substantially Equivalent
Regulation	892.1200

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View the full FDA submission: accessdata.fda.gov

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CARDIUS 3 X-ACT

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