K-number	K220062
Device name	QIAstat-Dx Gastrointestinal Panel 2
Applicant	QIAGEN GmbH
Product code	PCH
Device class	Class II
Decision date	May 31, 2024
Decision	Substantially Equivalent
Regulation	866.3990

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Source

View the full FDA submission: accessdata.fda.gov

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QIAstat-Dx Gastrointestinal Panel 2

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