DEVIN-NESTOR PNEUMATIC TOURNIQUET

DEVIN-NESTOR PNEUMATIC TOURNIQUET is an FDA 510(k)-cleared medical device (K780988) manufactured by Nestor Engineering Associates, Inc.. This device is classified under the General, Plastic Surgery specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on October 2, 1978. Regulation: 8.