K-number	K002294
Device name	BIOCHECK TESTOSTERONE EIA, MODEL BC-1115
Applicant	Biocheck, Inc.
Product code	CDZ
Device class	Class I
Decision date	Oct 2, 2000
Decision	Substantially Equivalent
Regulation	862.1680

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View the full FDA submission: accessdata.fda.gov

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BIOCHECK TESTOSTERONE EIA, MODEL BC-1115

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