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

QIAstat-Dx® Respiratory Panel Plus

K Number: K233100 · Decision May 10, 2024
Classifications
1
FEI Numbers
32
Registration Numbers
32
Same Product Code
32
Applicant Total
13
Review Days
227

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Basic Information

Device Name
QIAstat-Dx® Respiratory Panel Plus
K Number
K233100
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
September 26, 2023
Decision Date
May 10, 2024
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

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (QOF), ordered by most recent decision date.

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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
K250080 QIAstat-Dx Respiratory Panel Plus; QIAstat-Dx Respiratory Panel Mini
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
K183597 QIAstat-Dx Respiratory Panel
K133936 ARTUS C. DIFFICILE QS-RGQ MDX KIT
Search all 13 clearances from QIAGEN GmbH →