Zdrowie i gospodarka · 13/06/2000

FDA Classifies Subcutaneous, Implanted IV Infusion Port and Catheter for Personal Use Devices

The Food and Drug Administration (FDA) is classifying the subcutaneous, implanted, intravascular (IV) infusion port and catheter, and the percutaneous, implanted, long-term IV catheter intended for repeated vascular access into class II (special controls) to ensure the safety and effectiveness of these devices.