ACESSORY TO MODIFIED FREEDING JEJUNOSTO

ACESSORY TO MODIFIED FREEDING JEJUNOSTO is an FDA 510(k)-cleared medical device (K813504) manufactured by Midwest Metabolic Support Group. This device is classified under the Gastroenterology, Urology specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on January 6, 1982. Regulation: 8.