NXSTAGE PUREFLOW SL

NXSTAGE PUREFLOW SL is an FDA 510(k)-cleared medical device (K111174) 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 September 18, 2011. Regulation: 8.