KMK · Class I · 21 CFR 880.5210

FDA Product Code KMK: Device, Intravascular Catheter Securement

64
Total
64
Cleared
103d
Avg days
1977
Since

FDA 510(k) Cleared Device, Intravascular Catheter Securement Devices (Product Code KMK)

64 devices
1–24 of 64
No devices found for this product code.

About Product Code KMK - Regulatory Context