K-number	K013359
Device name	LP(A)-LATEX SEIKEN ASSAY KIT
Applicant	Denka Seiken'S
Product code	DFC
Device class	Class II
Decision date	Mar 8, 2002
Decision	Substantially Equivalent
Regulation	866.5600

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Source

View the full FDA submission: accessdata.fda.gov

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LP(A)-LATEX SEIKEN ASSAY KIT

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