← FDA DEVICE PRODUCT CODES

FDA PRODUCT CODE · UNCLASSIFIED

NWY — Test, Qualitative, Detection Of Dengue Igm And Igg Antibodies

Intended for the detection of IgM and IgG antibodies to dengue virus in human serum, plasma or whole blood.

DEVICE CLASS
Unclassified
MEDICAL SPECIALTY
Unknown
REVIEW PANEL
MI
— Implant— Life-sustaining— GMP-exempt— Third-party review eligible
0
510(K)/PMA CLEARANCES
0
RECALL ENTRIES

Related on SPEQ

Medical devices industry →Medical device quality (ISO 13485) →FDA device clearances →FDA enforcement & recalls →

Source: FDA device classification, 510(k)/PMA, and recall datasets (openFDA). Recall entries count distinct FDA recall numbers, so one recall event affecting several products appears as several entries. SPEQ is not affiliated with the FDA; this is a reference view of public FDA data.

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