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LIAISON PLEX Respiratory Flex Assay

Page Type
Cleared 510(K)
510(k) Number
K233410
510(k) Type
Traditional
Applicant
Luminex Corporation
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/1/2024
Days to Decision
147 days
Submission Type
Summary

LIAISON PLEX Respiratory Flex Assay

Page Type
Cleared 510(K)
510(k) Number
K233410
510(k) Type
Traditional
Applicant
Luminex Corporation
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/1/2024
Days to Decision
147 days
Submission Type
Summary