DeviceClearance

QIAstat-Dx Gastrointestinal Panel 2; QIAstat-Dx GI Panel 2 Mini B&V; QIAstat-Dx GI Panel 2 Mini B— 510(k) K252329

Substantially Equivalent

QIAGEN GmbH

FDA 510(k) clearance K252329 for QIAstat-Dx Gastrointestinal Panel 2; QIAstat-Dx GI Panel 2 Mini B&V; QIAstat-Dx GI Panel 2 Mini B, Substantially Equivalent on 2025-10-22. Applicant: QIAGEN GmbH.

Clearance details

Applicant
QIAGEN GmbH
Product code
Code PCH
Advisory panel
Microbiology
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Traditional
Location
Hilden, DE
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