KMI
- Product code
- KMI
- Device name
- Monitor, Bed Patient
- Device class
- Class 1
- 21 CFR
- 21 CFR 880.2400
- Medical specialty
- General Hospital
- Marketing pathway
- 510(K) Exempt
- 510(k) clearances (last 3 years)
- 31
Official FDA classification page: KMI
Classification and pathway per current FDA publications. Data from openFDA (CC0).