K-number	K211289
Device name	RMU-2000 Automated Chest Compression System
Applicant	Defibtech, LLC
Product code	DRM
Device class	Class II
Decision date	Nov 9, 2021
Decision	Substantially Equivalent
Regulation	870.5200

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Source

View the full FDA submission: accessdata.fda.gov

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RMU-2000 Automated Chest Compression System

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