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

LIAISON PLEX Respiratory Flex Assay

K Number: K233410 · Decision Mar 1, 2024
Classifications
1
FEI Numbers
32
Registration Numbers
32
Same Product Code
32
Applicant Total
15
Review Days
147

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Basic Information

Device Name
LIAISON PLEX Respiratory Flex Assay
K Number
K233410
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
866.3981
Medical Specialty
Microbiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Luminex Corporation
Date Received
October 6, 2023
Decision Date
March 1, 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 Luminex Corporation

K Number Device Name
K253722 LIAISON PLEX Gastrointestinal Flex Assay
K243490 LIAISON PLEX Gram-Positive Blood Culture Assay
K243013 LIAISON PLEX Gram-Negative Blood Culture Assay
K240627 LIAISON PLEX Yeast Blood Culture Assay
K191742 ARIES MRSA Assay
K172402 ARIES Group A Strep Assay, ARIES Group A Strep Assay Protocol File Kit
K171441 ARIES C. difficile Assay Complete Kit, ARIES C. difficile Assay Protocol File Kit, ARIES C. difficile Assay Kit (24 cassettes), ARIES Stool Resuspension Kit
K163626 ARIES Bordetella Assay; ARIES Bordetella Assay Protocol File Kit
K162772 ARIES GBS Assay
K161220 ARIES® Flu A/B & RSV Assay
Search all 15 clearances from Luminex Corporation →