K-number	K233932
Device name	Alinity i Toxo IgM
Applicant	Abbott Laboratories
Product code	LGD
Device class	Class II
Decision date	Aug 30, 2024
Decision	Substantially Equivalent
Regulation	866.3780

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Source

View the full FDA submission: accessdata.fda.gov

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Alinity i Toxo IgM

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