K-number	K022660
Device name	BIOCHECK MYOGLOBIN ELISA, MODEL BC-1117
Applicant	Biocheck, Inc.
Product code	DRR
Device class	Class II
Decision date	Dec 19, 2002
Decision	Substantially Equivalent
Regulation	870.2050

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View the full FDA submission: accessdata.fda.gov

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BIOCHECK MYOGLOBIN ELISA, MODEL BC-1117

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