K-number	K013062
Device name	BIOCHECK HUMAN CARDIAC TROPONIN-I IMMUNOASSAY TEST KIT
Applicant	Biocheck, Inc.
Product code	MMI
Device class	Class II
Decision date	Jan 8, 2002
Decision	Substantially Equivalent
Regulation	862.1215

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View the full FDA submission: accessdata.fda.gov

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BIOCHECK HUMAN CARDIAC TROPONIN-I IMMUNOASSAY TEST KIT

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