K-number	K130773
Device name	TEMPUS PRO PATIENT MONITOR
Applicant	Remote Diagnostic Technologies , Ltd.
Product code	MWI
Device class	Class II
Decision date	Jun 5, 2013
Decision	Substantially Equivalent
Regulation	870.2300

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Source

View the full FDA submission: accessdata.fda.gov

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TEMPUS PRO PATIENT MONITOR

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