K-number	K182668
Device name	Rapid Reboot Compression Therapy System
Applicant	Rapid Reboot Recovery Products, LLC
Product code	IRP
Device class	Class II
Decision date	Dec 14, 2018
Decision	Substantially Equivalent
Regulation	890.5650

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Source

View the full FDA submission: accessdata.fda.gov

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Rapid Reboot Compression Therapy System

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