K260333
- 510(k) number
- K260333
- Device name
- LIAISON NES Group A Strep; LIAISON NES Group A Strep Control Swab Kit
- Applicant
- Diasorin Molecular, LLC CA · US
- Product code
- PGX — Groups A, C And G Beta-Hemolytic Streptococcus Nucle
- Decision date
- 2026-06-15
- Date received
- 2026-02-02
- Decision
- Substantially Equivalent
- Clearance type
- Dual Track
- Advisory committee
- Microbiology
PDFDownload 510(k) SummaryArchived here · 0.7 MB · U.S. public domain
Also available from FDA: K260333.pdf
Official FDA record: K260333
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.