NWG
- Product code
- NWG
- Device name
- Autoantibodies, Glutamic Acid Decarboxylase (Gad)
- Device class
- Class 2
- 21 CFR
- 21 CFR 866.5660
- Medical specialty
- Immunology
- Marketing pathway
- 510(K)
- Flag
- Third-party review eligible
- 510(k) clearances (all years, FDA)
- 2 (all years; only the last 3 years are listed here)
FDA classification definition
The device is used for the semi-quantitative determination of glutamic acid decarboxylase (GAD) autoantibodies in human serum as an aid in the diagnosis of Type I diabetes mellitus (autoimmune mediated diabetes).
Official FDA classification page: NWG
Classification and pathway per current FDA publications. Data from openFDA (CC0).