K-number	K023853
Device name	K-ASSAY LP(A) CONTROLS
Applicant	Kamiya Biomedical Co.
Product code	DFC
Device class	Class II
Decision date	Dec 13, 2002
Decision	Substantially Equivalent
Regulation	866.5600

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View the full FDA submission: accessdata.fda.gov

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K-ASSAY LP(A) CONTROLS

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