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FDA 510(k)

QIAstat-Dx BCID GPF Plus AMR Panel

K-Number: K254194 · 2026-08-06

ApplicantQIAGEN GmbH
Decision Date2026-08-06
Product CodePAM
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

QIAstat-Dx BCID GPF Plus AMR Panel is the device name listed in this FDA 510(k) record. The listed applicant is QIAGEN GmbH. It received FDA 510(k) clearance on 2026-08-06 under 510(k) number K254194. The device is classified under product code PAM. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the QIAstat-Dx BCID GPF Plus AMR Panel?

QIAstat-Dx BCID GPF Plus AMR Panel is a medical device that received FDA 510(k) clearance on 2026-08-06. The listed applicant is QIAGEN GmbH. The 510(k) number is K254194.

When did QIAstat-Dx BCID GPF Plus AMR Panel receive FDA 510(k) clearance?

QIAstat-Dx BCID GPF Plus AMR Panel received FDA 510(k) clearance on 2026-08-06, under 510(k) number K254194.

Who is the listed applicant for QIAstat-Dx BCID GPF Plus AMR Panel?

The FDA 510(k) record lists QIAGEN GmbH as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for QIAstat-Dx BCID GPF Plus AMR Panel?

The FDA product code for QIAstat-Dx BCID GPF Plus AMR Panel is PAM.

Other records listing QIAGEN GmbH as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

PMA P180043Somatic gene mutation detection systemK254032QIAstat-Dx Gastrointestinal Panel 2; QIAstat-Dx GI Panel 2 Mini B&V; QIAstat-Dx GI Panel 2 Mini BPMA P010033TEST, IMMUNITY, CELL MEDIATED, MYCOBACTERIUM TUBERCULOSISPMA P190001Somatic gene mutation detection systemK252329QIAstat-Dx Gastrointestinal Panel 2; QIAstat-Dx GI Panel 2 Mini B&V; QIAstat-Dx GI Panel 2 Mini BK250080QIAstat-Dx Respiratory Panel Plus; QIAstat-Dx Respiratory Panel Mini

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Related Devices (Code: PAM)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K243490LIAISON PLEX Gram-Positive Blood Culture AssayLuminex CorporationK181663ePlex Blood Culture Identification Panel - Gram Positive (BCID-GP) PanelGenmark Diagnostics, IncorporatedK163390iC-GPC Assay TM for use on the iC-SystemTMIcubate, Inc.K152470Great Basin Staph ID/R Blood Culture PanelGreat Basin Scientific, Inc.

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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