K233410
- 510(k) number
- K233410
- Device name
- LIAISON PLEX Respiratory Flex Assay
- Applicant
- Luminex Corporation IL · US
- Product code
- QOF — Multi-Target Respiratory Specimen Nucleic Acid Test
- Decision date
- 2024-03-01
- Date received
- 2023-10-06
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Microbiology
PDFDownload 510(k) SummaryArchived here · 3.0 MB · U.S. public domain
Also available from FDA: K233410.pdf
Official FDA record: K233410
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.