K-number	K832383
Device name	IDT ANA STIQ ASSAY
Applicant	Intl. Diagnostic Technology
Product code	DHN
Device class	Class II
Decision date	Aug 31, 1983
Decision	Substantially Equivalent
Regulation	866.5100

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View the full FDA submission: accessdata.fda.gov

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IDT ANA STIQ ASSAY

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