KMK · Class I · 21 CFR 880.5210

FDA Product Code KMK: Device, Intravascular Catheter Securement

Leading manufacturers include Johnson & Johnson Professionals, Inc., Bd Becton Dickinson Vacutainer Systems Preanalytic and Interrad Medical, Inc..

64
Total
64
Cleared
103d
Avg days
1977
Since
64 devices
25–48 of 64
No devices found for this product code.