FDA 510(k) FDA class 2 Substantially Equivalent 🇩🇪 Germany

QIAstat-Dx Respiratory Panel Plus; QIAstat-Dx Respiratory Panel Mini

K Number: K250080 · Decision Aug 27, 2025
Classifications
1
FEI Numbers
32
Registration Numbers
32
Same Product Code
32
Applicant Total
13
Review Days
226

Basic Information

Device Name
QIAstat-Dx Respiratory Panel Plus; QIAstat-Dx Respiratory Panel Mini
K Number
K250080
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
866.3981
Medical Specialty
Microbiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
QIAGEN GmbH
Date Received
January 13, 2025
Decision Date
August 27, 2025
Product Code
QOF
Advisory Committee
Microbiology
Review Advisory Committee
MI
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
QOF Multi-Target Respiratory Specimen Nucleic Acid Test Including Sars-Cov-2 And Other Microbial Agents

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Other Clearances by QIAGEN GmbH

K Number Device Name
K254032 QIAstat-Dx Gastrointestinal Panel 2; QIAstat-Dx GI Panel 2 Mini B&V; QIAstat-Dx GI Panel 2 Mini B
K252329 QIAstat-Dx Gastrointestinal Panel 2; QIAstat-Dx GI Panel 2 Mini B&V; QIAstat-Dx GI Panel 2 Mini B
K250324 QIAstat-Dx GI Panel 2 Mini B
K243813 QIAstat-Dx GI Panel 2 Mini B&V
K242256 QIAstat-Dx Meningitis/Encephalitis (ME) Panel
K242353 QIAstat-Dx Respiratory Panel Mini
K220062 QIAstat-Dx Gastrointestinal Panel 2
K233100 QIAstat-Dx® Respiratory Panel Plus
K183597 QIAstat-Dx Respiratory Panel
K133936 ARTUS C. DIFFICILE QS-RGQ MDX KIT
Search all 13 clearances from QIAGEN GmbH →