FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

Xpert Xpress CoV-2/Flu/RSV plus

K Number: K242071 · Decision Jan 10, 2025
Classifications
1
FEI Numbers
32
Registration Numbers
32
Same Product Code
32
Applicant Total
50
Review Days
178

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Basic Information

Device Name
Xpert Xpress CoV-2/Flu/RSV plus
K Number
K242071
Device Class
FDA class 2
Clearance Type
Dual Track
Regulation Number
866.3981
Medical Specialty
Microbiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Cepheid
Date Received
July 16, 2024
Decision Date
January 10, 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 510(k) clearances with the same product code (QOF), ordered by most recent decision date.

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Other Clearances by Cepheid

K Number Device Name
K253653 Xpert Hemorrhagic Fever
K251721 Xpert GI Panel
K250218 Xpert® FII & FV
DEN240016 Xpert HCV; GeneXpert Xpress System
K231381 Xpert Xpress MVP; GeneXpert Xpress System
K222638 Xpert® Xpress GBS, GeneXpert® Dx System, GeneXpert® Infinity Systems
K221160 Xpert Xpress MVP, GeneXpert Dx System, GeneXpert Infinity System
K203429 Xpert GBS LB XC, GeneXpert Dx System, GeneXpert Infinity System
K212213 Xpert Xpress MVP, GeneXpert Dx System, GeneXpert Infinity System
K190076 Xpert BCR-ABL Ultra, GeneXpert Dx System, GeneXpert Infinity-48s and GeneXpert Infinity-80 Systems
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