K-number	K211235
Device name	CIRCUL8 Luxe DVT Prevention Device
Applicant	Ortho8, Inc.
Product code	JOW
Device class	Class II
Decision date	Sep 8, 2021
Decision	Substantially Equivalent
Regulation	870.5800

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Source

View the full FDA submission: accessdata.fda.gov

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CIRCUL8 Luxe DVT Prevention Device

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