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

QIAstat-Dx Respiratory Panel Mini

K Number: K242353 · Decision Oct 25, 2024
Classifications
1
FEI Numbers
32
Registration Numbers
32
Same Product Code
32
Applicant Total
13
Review Days
78

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Basic Information

Device Name
QIAstat-Dx Respiratory Panel Mini
K Number
K242353
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
866.3981
Medical Specialty
Microbiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
QIAGEN GmbH
Date Received
August 8, 2024
Decision Date
October 25, 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
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 →