April 9, 2008 11:56 AM Dori Schatell The Baby K was on the market--approved by the FDA--for years. When the Aksys PHD machine was designed as a home-only machine, they had to jump through an additional hoop: a study of the machine in the home to be sure it was safe. So, that machine got a home dialysis approval. Having one machine with a home dialysis approval raised the bar for other home HD machines. So, when the NxStage System One machine came on the market (for use in acute dialysis--and at home), they did a home study to get both regular approval and home approval. The Allient Sorbent machine by Renal Solutions is doing the same. Probably Fresenius thought the Baby K was "grandfathered" in, because it had been on the market prior to the Aksys PHD. Apparently the FDA disagreed, so now they may jump through that hoop. have no idea if they are looking at the Baby K for daily or nocturnal in particular--the issue is home.
The 2008K@home incorporates all standard performance and safety features expected in modern hemodialysis machines. The 2008K@home will be available to patients in the late spring/early summer, 2011.