ASI Plethysmogrpah Analyzer

ASI Plethysmogrpah Analyzer is an FDA 510(k)-cleared medical device (K200567) manufactured by Arterial Stiffness, Inc.. This device is classified under the Cardiovascular specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on February 25, 2021. Regulation: 8.