K-number	K903367
Device name	KETONE TEST A SANWA STANDARD
Applicant	Ihara Medics U.S., Inc.
Product code	JIN
Device class	Class I
Decision date	Nov 20, 1990
Decision	Substantially Equivalent
Regulation	862.1435

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View the full FDA submission: accessdata.fda.gov

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KETONE TEST A SANWA STANDARD

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