K-number	K213875
Device name	DRI TM Tricyclics Serum Tox Assay
Applicant	Microgenics Corporation
Product code	LFH
Device class	Class II
Decision date	Dec 21, 2022
Decision	Substantially Equivalent
Regulation	862.3910

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Source

View the full FDA submission: accessdata.fda.gov

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DRI TM Tricyclics Serum Tox Assay

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