PAS ALCOVISOR MARS, PAS ALCOVISOR SATELLITE

PAS ALCOVISOR MARS, PAS ALCOVISOR SATELLITE is an FDA 510(k)-cleared medical device (K123470) manufactured by Pas Systems International, Inc.. This device is classified under the Clinical Toxicology specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on April 28, 2013. Regulation: 8.