K-number	K221654
Device name	medi pneumatic compression system (pcs)-genius (Model 652)
Applicant	Medi USA, LP
Product code	JOW
Device class	Class II
Decision date	Jul 7, 2022
Decision	Substantially Equivalent
Regulation	870.5800

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View the full FDA submission: accessdata.fda.gov

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medi pneumatic compression system (pcs)-genius (Model 652)

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