Aksys, Ltd. is one of 16278 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Aksys, Ltd. - FDA 510(k) Cleared Devices
Recent clearances: PHD PERSONAL HEMODIALYSIS INSTRUMENT-1M101, PHD WATER PRE-TREATMENT KIT-1W605,PHD HARD PLUMBING KIT-1W604, PHD BLOOD TUB
1
Total
1
Cleared
0
Denied
Aksys, Ltd. has 1 FDA 510(k) cleared medical devices. Based in Lincolnshire, US.
Historical record: 1 cleared submissions from 2002 to 2002. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Aksys, Ltd. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Aksys, Ltd.
1 devices