
Pas Systems International, Inc.
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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.