THE HOMMED SENTRY, MODEL 1 SENTRY

THE HOMMED SENTRY, MODEL 1 SENTRY is an FDA 510(k)-cleared medical device (K993938) manufactured by Hommed, 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 March 14, 2000. Regulation: 8.