KFL
- Product code
- KFL
- Device name
- Microtome, Sliding
- Device class
- Class 1
- 21 CFR
- 21 CFR 864.3010
- Medical specialty
- Pathology
- Marketing pathway
- 510(K) Exempt
- Flag
- GMP exempt
Official FDA classification page: KFL
Classification and pathway per current FDA publications. Data from openFDA (CC0).