K-number	K201746
Device name	Tempus Pro Patient Monitor
Applicant	Remote Diagnostic Technologies Limited
Product code	MHX
Device class	Class II
Decision date	Sep 18, 2020
Decision	Substantially Equivalent
Regulation	870.1025

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Source

View the full FDA submission: accessdata.fda.gov

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Tempus Pro Patient Monitor

Everything you need for a 510(k) submission. Nothing you don't.