K-number	K203745
Device name	AURORA Evacuator +Coag
Applicant	Rebound Therapeutics
Product code	GEI
Device class	Class II
Decision date	Dec 2, 2021
Decision	Substantially Equivalent
Regulation	878.4400

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Source

View the full FDA submission: accessdata.fda.gov

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AURORA Evacuator +Coag

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