GMA
- Product code
- GMA
- Device name
- Antisera, Fluorescent, Sporothrix Schenekii
- Device class
- Class 1
- 21 CFR
- 21 CFR 866.3680
- Medical specialty
- Microbiology
- Marketing pathway
- 510(K) Exempt
- 510(k) clearances (last 3 years)
- 1
Official FDA classification page: GMA
Classification and pathway per current FDA publications. Data from openFDA (CC0).