KMI · Class I · 21 CFR 880.2400

FDA Product Code KMI: Monitor, Bed Patient

31
Total
31
Cleared
130d
Avg days
1977
Since

FDA 510(k) Cleared Monitor, Bed Patient Devices (Product Code KMI)

31 devices
1–24 of 31
No devices found for this product code.

About Product Code KMI - Regulatory Context