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FDA 510(k)

QIAstat-Dx GI Panel 2 Mini B

K-Number: K250324 · 2025-02-28

ApplicantQIAGEN GmbH
Decision Date2025-02-28
Product CodePCH
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

QIAstat-Dx GI Panel 2 Mini B is a medical device manufactured by QIAGEN GmbH. It received FDA 510(k) clearance on 2025-02-28 under approval number K250324. The device is classified under product code PCH. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the QIAstat-Dx GI Panel 2 Mini B?

QIAstat-Dx GI Panel 2 Mini B is a medical device that received FDA 510(k) clearance on 2025-02-28. It is manufactured by QIAGEN GmbH. The 510(k) number is K250324.

When was QIAstat-Dx GI Panel 2 Mini B approved by the FDA?

QIAstat-Dx GI Panel 2 Mini B received FDA 510(k) clearance on 2025-02-28, under approval number K250324.

What company makes QIAstat-Dx GI Panel 2 Mini B?

QIAstat-Dx GI Panel 2 Mini B is manufactured by QIAGEN GmbH.

What is the FDA product code for QIAstat-Dx GI Panel 2 Mini B?

The FDA product code for QIAstat-Dx GI Panel 2 Mini B is PCH.

Other Devices by QIAGEN GmbH

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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