K-number	K012040
Device name	RAMP MYOGLOBIN ASSAY
Applicant	Response Biomedical Corp.
Product code	DDR
Device class	Class II
Decision date	Dec 18, 2001
Decision	Substantially Equivalent
Regulation	866.5680

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View the full FDA submission: accessdata.fda.gov

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RAMP MYOGLOBIN ASSAY

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