K-number	K811808
Device name	AUTOPAK-12 FERRITIN KIT
Applicant	Micromedic Systems
Product code	DBF
Device class	Class II
Decision date	Jul 10, 1981
Decision	Substantially Equivalent
Regulation	866.5340

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View the full FDA submission: accessdata.fda.gov

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AUTOPAK-12 FERRITIN KIT

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