K-number	K001552
Device name	TREPCHEK TREPONEMAL ANTIBODY EIA
Applicant	Phoenix Biotech Corp.
Product code	LIP
Device class	Class II
Decision date	Oct 19, 2000
Decision	Substantially Equivalent
Regulation	866.3830

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View the full FDA submission: accessdata.fda.gov

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TREPCHEK TREPONEMAL ANTIBODY EIA

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