Nipro Renal Solutions USA, Corp. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Nipro Renal Solutions USA, Corp. - FDA 510(k) Cleared Devices
Recent clearances: Citric Complete Liquid Citric Acid Concentrate, Nipro Dry Complete Dry Acid Concentrate for Hemodialysis
2
Total
2
Cleared
0
Denied
Nipro Renal Solutions USA, Corp. has 2 FDA 510(k) cleared medical devices. Based in Lewisberry, US.
Last cleared in 2023. Active since 2020. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Nipro Renal Solutions USA, Corp. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Mcnees Wallace & Nurick, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Nipro Renal Solutions USA, Corp.
2 devices