NxStage PureFlow Solution

NxStage PureFlow Solution is an FDA 510(k)-cleared medical device (K233213) manufactured by Nxstage Medical, Inc.. This device is classified under the Gastroenterology, Urology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on January 17, 2024. Regulation: 8.