K-number	K220583
Device name	ClearCheck Model RADCC V2
Applicant	Radformation, Inc.
Product code	IYE
Device class	Class II
Decision date	Aug 23, 2022
Decision	Substantially Equivalent
Regulation	892.5050

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Source

View the full FDA submission: accessdata.fda.gov

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ClearCheck Model RADCC V2

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