CDC Human Influenza Virus Real-Time RT-PCR Diagnostic Panel, Influenza A Subtyping Kit (Ver4)— 510(k) K241110
Substantially EquivalentCenters for Disease Control and Prevention
FDA 510(k) clearance K241110 for CDC Human Influenza Virus Real-Time RT-PCR Diagnostic Panel, Influenza A Subtyping Kit (Ver4), Substantially Equivalent on 2024-05-21. Applicant: Centers for Disease Control and Prevention.
Clearance details
- Applicant
- Centers for Disease Control and Prevention
- Product code
- Code OZE
- Advisory panel
- Microbiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Location
- Atlanta, GA, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.