Nephros is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Nephros - FDA 510(k) Cleared Devices
Recent clearances: HDF Assist Mudule, HDF Infusion Set and Substitution Filter
1
Total
1
Cleared
0
Denied
Nephros has 1 FDA 510(k) cleared medical devices. Based in South Orange, US.
Last cleared in 2022. Active since 2022. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Nephros Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Nephros
1 devices