HemoSphere Advanced Monitor, HemoSphere Pressure Cable

HemoSphere Advanced Monitor, HemoSphere Pressure Cable is an FDA 510(k)-cleared medical device (K180881) manufactured by Edwards Lifesciences, LLC. This device is classified under the Cardiovascular specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on November 15, 2018. Regulation: 8.