K-number	K233976
Device name	VasoGuard (V10, V8, V6, V4, V2)
Applicant	Corvascular Diagnostics, LLC
Product code	JOP
Device class	Class II
Decision date	Jul 19, 2024
Decision	Substantially Equivalent
Regulation	870.2880

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View the full FDA submission: accessdata.fda.gov

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VasoGuard (V10, V8, V6, V4, V2)

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