KDM
- Product code
- KDM
- Device name
- Sigmoidoscope, Rigid, Non-Electrical
- Device class
- Class 2
- 21 CFR
- 21 CFR 876.1500
- Medical specialty
- Gastroenterology, Urology
- Marketing pathway
- 510(K)
- 510(k) clearances (all years, FDA)
- 1 (all years; only the last 3 years are listed here)
Official FDA classification page: KDM
Classification and pathway per current FDA publications. Data from openFDA (CC0).