GOK
- Product code
- GOK
- Device name
- Antisera, Hai (Including Hai Control), Rubella
- Device class
- Class 2
- 21 CFR
- 21 CFR 866.3510
- Medical specialty
- Microbiology
- Marketing pathway
- 510(K)
- Flag
- Third-party review eligible
- 510(k) clearances (last 3 years)
- 11
Official FDA classification page: GOK
Classification and pathway per current FDA publications. Data from openFDA (CC0).