FIP · Class II · 21 CFR 876.5665

FDA Product Code FIP: Subsystem, Water Purification

FDA product code FIP covers water purification subsystems used in hemodialysis.

These systems process tap water through reverse osmosis, deionization, and other purification steps to produce water meeting strict AAMI standards for hemodialysis fluid preparation. Ultrapure water is critical to preventing dialysis-related complications caused by endotoxins and contaminants.

FIP devices are Class II medical devices, regulated under 21 CFR 876.5665 and reviewed by the FDA Gastroenterology & Urology panel.

Leading manufacturers include Fresenius Medical Care Renal Therapies Group, LLC, Baxter Healthcare Corporation and B.Braun Medical, Inc..

117
Total
117
Cleared
225d
Avg days
1977
Since
117 devices
73–96 of 117
No devices found for this product code.