AESCULAP POWER SYSTEMS (ELAN-E & MICROTRON)

AESCULAP POWER SYSTEMS (ELAN-E & MICROTRON) is an FDA 510(k)-cleared medical device (K953968) manufactured by Aesculap, Inc.. This device is classified under the General, Plastic Surgery specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on February 4, 1996. Regulation: 8.