GTE
- Product code
- GTE
- Device name
- Antisera, Arizona Spp., All
- Device class
- Class 1
- 21 CFR
- 21 CFR 866.3035
- Medical specialty
- Microbiology
- Marketing pathway
- 510(K) Exempt
Official FDA classification page: GTE
Classification and pathway per current FDA publications. Data from openFDA (CC0).