K-number	K993444
Device name	K-ASSAY ALPHA-1 AT
Applicant	Kamiya Biomedical Co.
Product code	DEM
Device class	Class II
Decision date	Nov 24, 1999
Decision	Substantially Equivalent
Regulation	866.5130

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View the full FDA submission: accessdata.fda.gov

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K-ASSAY ALPHA-1 AT

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