SPLINT, PNEUMATIC, ARM & SPLINT, PNEUMATIC, LEG

SPLINT, PNEUMATIC, ARM & SPLINT, PNEUMATIC, LEG is an FDA 510(k)-cleared medical device (K941869) manufactured by The Lighthouse For the Blind, Inc.. This device is classified under the General Hospital specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on August 2, 1994. Regulation: 8.