K-number	K840006
Device name	KINETIC LDH, A< BLUE 610 METHOD
Applicant	American Monitor Corp.
Product code	CFJ
Device class	Class II
Decision date	Mar 23, 1984
Decision	Substantially Equivalent
Regulation	862.1440

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View the full FDA submission: accessdata.fda.gov

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KINETIC LDH, A< BLUE 610 METHOD

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