K-number	K233946
Device name	IMMULITE® 2000 BR-MA
Applicant	Siemens Healthcare Diagnostics Products, Ltd.
Product code	MOI
Device class	Class II
Decision date	Mar 13, 2024
Decision	Substantially Equivalent
Regulation	866.6010

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Source

View the full FDA submission: accessdata.fda.gov

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IMMULITE® 2000 BR-MA

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