K-number	K141809
Device name	RMU-1000 AUTOMATED CHEST COMPRESSION SYSTEM
Applicant	Defibtech, LLC
Product code	DRM
Device class	Class II
Decision date	Oct 27, 2014
Decision	Substantially Equivalent
Regulation	870.5200

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Source

View the full FDA submission: accessdata.fda.gov

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RMU-1000 AUTOMATED CHEST COMPRESSION SYSTEM

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