FDA Registration Active 🇺🇸 United States

LIAISON PLEX Respiratory Flex Assay

Reg #: 3006028115 · FEI: 3006028115 · Expires 2025
Products
10
Proprietary Names
1
Establishment Types
1
Classifications
10

Registration Details

Registration Name
Luminex Corporation
Registration Number
3006028115
FEI Number
3006028115
Status
Active
Expiry Year
2025
Initial Importer
No
Address
4088 Commercial Avenue
City
Northbrook
State
IL
ZIP
60062
Country
US

Regulatory Submissions

510(k) Number
K233410

Owner / Operator

Firm Name
Luminex Corporation
Operator Number
9032042
Address
12212 Technology Blvd.
City
Austin
State
TX
Postal Code
78727
Country
US
Correspondent
Mari Meyer

Products

Device Name Product Code
Respiratory Virus Panel Nucleic Acid Assay System OCC
Non-Sars Coronavirus Multiplex Nucleic Acid Assay OTG
Multi-Target Respiratory Specimen Nucleic Acid Test Including Sars-Cov-2 And Other Microbial Agents QOF
Human Metapneumovirus (Hmpv) Rna Assay System OEM
Influenza A And Influenza B Multiplex Nucleic Acid Assay OZE
Parainfluenza Multiplex Nucleic Acid Assay OOU
Mycoplasma Pneumoniae Dna Assay System OZX
Bordetella Pertussis Dna Assay System OZZ
Instrumentation For Clinical Multiplex Test Systems NSU
Chlamydophila Pneumoniae Dna Assay System OZY

Proprietary Names

LIAISON PLEX Respiratory Flex Assay

Establishment Types

Manufacture Medical Device