K-number	K192240
Device name	RAPIDPoint 500e Blood Gas System
Applicant	Siemens Healthcare Diagnostics, Inc.
Product code	CHL
Device class	Class II
Decision date	Mar 27, 2020
Decision	Substantially Equivalent
Regulation	862.1120

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View the full FDA submission: accessdata.fda.gov

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RAPIDPoint 500e Blood Gas System

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