K-number	K231616
Device name	ZEUS IFA(TM) nDNA Test System, ZEUS dIFine
Applicant	Zeus Scientific
Product code	KTL
Device class	Class II
Decision date	Aug 31, 2023
Decision	Substantially Equivalent
Regulation	866.5100

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Source

View the full FDA submission: accessdata.fda.gov

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ZEUS IFA(TM) nDNA Test System, ZEUS dIFine

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