GML
- Product code
- GML
- Device name
- Antisera, Fluorescent, Histoplasma Capsulatum
- Device class
- Class 2
- 21 CFR
- 21 CFR 866.3320
- Medical specialty
- Microbiology
- Marketing pathway
- 510(K) Exempt
Official FDA classification page: GML
Classification and pathway per current FDA publications. Data from openFDA (CC0).