510(k) clearances

CDC Human Influenza Virus Real-Time RT-PCR Diagnostic Panel, Influenza A Subtyping Kit (Ver4)

Centers for Disease Control and Prevention · Microbiology

K241110Substantially EquivalentSpecialOZE
Open FDA's page for this record
Third party flag
N
City
Atlanta
Advisory committee description
Microbiology
Address 1
1600 Clifton Rd., NE
Address 2
Ms G36
Statement or summary
Summary
Product code
OZE
Zip code
30329
Applicant
Centers for Disease Control and Prevention
Decision date
2024-05-21
Decision code
SESE
Country code
US
Device name
CDC Human Influenza Virus Real-Time RT-PCR Diagnostic Panel, Influenza A Subtyping Kit (Ver4)
Advisory committee
MI
Contact
John Barnes
K number
K241110
State
GA
Date received
2024-04-22
Review advisory committee
MI
Postal code
30329
Decision description
Substantially Equivalent
Clearance type
Special
Harmonized identifiers (openFDA)
Device name
Influenza A And Influenza B Multiplex Nucleic Acid Assay
Medical specialty description
Microbiology
Regulation number
866.3980
Device class
2
Registration number
1528450, 3005360469, 2243471, 3003795116, 3003018722, 1050190, 3002773840, 3013019728, 3004141078, 3023999024, 1221359, 3006028115, 3012494290, 3038610665, 9610126, 1650733, 3008632402, 3029059580, 3023372670, 3010770794, 3007799234
FEI number
2243471, 3003795116, 3003018722, 1050190, 3005670738, 3002773840, 3002524000, 3002806559, 3013019728, 3004141078, 3023999024, 1221359, 3006028115, 3012494290, 3038610665, 3008632402, 3029059580, 3023372670, 3010770794, 3007799234, 1000122536
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Data from openFDA, FDA's public API. FDA says not to rely on it to make decisions about medical care and to treat every result as unvalidated; confirm against FDA's own record and the product labeling. Not medical or legal advice.