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. Device class: 2.
Clearance details
- Applicant
- Centers for Disease Control and Prevention
- Product code
- Product code OZE
- Device class
- Class 2
- Regulation
- 21 CFR 866.3980
- Advisory panel
- Microbiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Location
- Atlanta, GA, US
Recent devices under product code OZE
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More clearances from Centers for Disease Control and Prevention
view allData sourced from openFDA. This site is unofficial and independent of the FDA.