KMH
- Product code
- KMH
- Device name
- Sterilizer, Dry Heat
- Device class
- Class 2
- 21 CFR
- 21 CFR 880.6870
- Medical specialty
- General Hospital
- Marketing pathway
- 510(K)
- Flag
- Third-party review eligible
- 510(k) clearances (last 3 years)
- 10
Official FDA classification page: KMH
Classification and pathway per current FDA publications. Data from openFDA (CC0).