K-number	K810002
Device name	'NO-BOIL' VITAMIN B12 KIT
Applicant	Diagnostic Products Corp.
Product code	CDD
Device class	Class II
Decision date	Jan 16, 1981
Decision	Substantially Equivalent
Regulation	862.1810

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View the full FDA submission: accessdata.fda.gov

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'NO-BOIL' VITAMIN B12 KIT

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