MODIFICATION IN MEMBRANE HOUSING CONFI

MODIFICATION IN MEMBRANE HOUSING CONFI is an FDA 510(k)-cleared medical device (K832925) manufactured by Ries Biologicals. 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 November 27, 1983. Regulation: 8.