Anivia SG1000 Pump Console

Anivia SG1000 Pump Console is an FDA 510(k)-cleared medical device (K230698) manufactured by Apmtd, 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 April 17, 2023. Regulation: 8.