K-number	K902219
Device name	KRONAMAX HUMAN PERFORMANCE LAB
Applicant	Physicians Digital Co.
Product code	IKK
Device class	Class II
Decision date	Jul 25, 1990
Decision	Substantially Equivalent
Regulation	890.1925

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View the full FDA submission: accessdata.fda.gov

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KRONAMAX HUMAN PERFORMANCE LAB

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