K-number	K200849
Device name	Tempus LS - Manual
Applicant	Remote Diagnostic Technologies, Ltd. A Philips Company
Product code	LDD
Device class	Class II
Decision date	Jul 24, 2020
Decision	Substantially Equivalent
Regulation	870.5300

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Source

View the full FDA submission: accessdata.fda.gov

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Tempus LS - Manual

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