KIO
- Product code
- KIO
- Device name
- Slide Stainer, Immersion Type
- Device class
- Class 1
- 21 CFR
- 21 CFR 864.3800
- Medical specialty
- Pathology
- Marketing pathway
- 510(K) Exempt
- 510(k) clearances (last 3 years)
- 1
Official FDA classification page: KIO
Classification and pathway per current FDA publications. Data from openFDA (CC0).