GMX
- Product code
- GMX
- Device name
- Antisera, Fluorescent Antibody For Fta-Abs Test
- Device class
- Class 2
- 21 CFR
- 21 CFR 866.3830
- Medical specialty
- Microbiology
- Marketing pathway
- 510(K)
- Flag
- Third-party review eligible
Official FDA classification page: GMX
Classification and pathway per current FDA publications. Data from openFDA (CC0).