Product code NWY

Device name
Test, Qualitative, Detection Of Dengue Igm And Igg Antibodies
Medical specialty
Unknown
Device class
N
Review panel
MI
Implant
N
Life sustaining/supporting
N
GMP exempt
N
Third party review
N
Summary malfunction reporting
Eligible
Definition
Intended for the detection of IgM and IgG antibodies to dengue virus in human serum, plasma or whole blood.
Source
FDA openFDA device classification dataset