KIX
- Product code
- KIX
- Device name
- Media, Mycoplasma Detection
- Device class
- Class 1
- 21 CFR
- 21 CFR 864.2360
- Medical specialty
- Hematology
- Marketing pathway
- 510(K) Exempt
Official FDA classification page: KIX
Classification and pathway per current FDA publications. Data from openFDA (CC0).