K-number	K183637
Device name	Cruxcan (CRX-1000)
Applicant	Cruxell Corp.
Product code	MUH
Device class	Class II
Decision date	Feb 12, 2019
Decision	Substantially Equivalent
Regulation	872.1800

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View the full FDA submission: accessdata.fda.gov

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Cruxcan (CRX-1000)

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