GWD
- Product code
- GWD
- Device name
- Indirect Fluorescent Antibody Test, Entamoeba Histolytica & Rel Sp
- Device class
- Class 2
- 21 CFR
- 21 CFR 866.3220
- Medical specialty
- Microbiology
- Marketing pathway
- 510(K) Exempt
- 510(k) clearances (last 3 years)
- 2
Official FDA classification page: GWD
Classification and pathway per current FDA publications. Data from openFDA (CC0).