K-number	K082539
Device name	MASTERSCOPE, MASTERSCOPE ECG, MASTERSCOPE CT
Applicant	Cardinal Health Germany 234 GmbH
Product code	BTY
Device class	Class II
Decision date	Dec 2, 2008
Decision	Substantially Equivalent
Regulation	868.1890

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View the full FDA submission: accessdata.fda.gov

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MASTERSCOPE, MASTERSCOPE ECG, MASTERSCOPE CT

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