K-number	K192169
Device name	PulsioFlex Monitoring System with ProAQT Sensor
Applicant	Pulsion Medical Systems SE
Product code	DXG
Device class	Class II
Decision date	Apr 30, 2020
Decision	Substantially Equivalent
Regulation	870.1435

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Source

View the full FDA submission: accessdata.fda.gov

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PulsioFlex Monitoring System with ProAQT Sensor

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