Clearance Summary
FRESENIUS 2008K HOME HEMODIALYSIS MACHINE WITH WIRELESS WETNESS DETECTOR (WETALERT) received FDA 510(k) clearance under submission number K121421, sponsored by Fresenius Medical Care North America, Design Cente. The device was reviewed via the Special premarket notification pathway and assigned to the Gastroenterology, Urology review panel. The statutory decision date of record is 2013-01-17.
- Submission: K121421
- Applicant / Sponsor: Fresenius Medical Care North America, Design Cente
- Clearance pathway: Special
- Review panel: Gastroenterology, Urology
- Device class: Class II
- Regulation citation: 21 CFR 876.5860
- Decision date: 2013-01-17
Classification & Regulation
This clearance is catalogued under FDA product code ONW and 21 CFR 876.5860, within the Gastroenterology, Urology review panel as a Class II device.