K-number	K782125
Device name	RIA KIT, KANAMYCIN
Applicant	Diagnostic Products Corp.
Product code	KJI
Device class	Class II
Decision date	Jan 10, 1979
Decision	Substantially Equivalent
Regulation	862.3520

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View the full FDA submission: accessdata.fda.gov

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RIA KIT, KANAMYCIN

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