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

QIAstat-Dx Respiratory Panel

K Number: K183597 · Decision May 18, 2019
Classifications
1
FEI Numbers
32
Registration Numbers
32
Same Product Code
78
Applicant Total
13
Review Days
148

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Basic Information

Device Name
QIAstat-Dx Respiratory Panel
K Number
K183597
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
866.3980
Medical Specialty
Microbiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
QIAGEN GmbH
Date Received
December 21, 2018
Decision Date
May 18, 2019
Product Code
OCC
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
OCC Respiratory Virus Panel Nucleic Acid Assay System

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (OCC), 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
K233100 QIAstat-Dx® Respiratory Panel Plus
K133936 ARTUS C. DIFFICILE QS-RGQ MDX KIT
Search all 13 clearances from QIAGEN GmbH →