K-number	K213081
Device name	CLISIS SYSTEMS, Discovery RF180
Applicant	General Medical Merate S.P.A
Product code	IZF
Device class	Class II
Decision date	Oct 26, 2021
Decision	Substantially Equivalent
Regulation	892.1740

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Source

View the full FDA submission: accessdata.fda.gov

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CLISIS SYSTEMS, Discovery RF180

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