HOMMED SENTRY IIIB-F PATIENT MONITOR SYSTEM

HOMMED SENTRY IIIB-F PATIENT MONITOR SYSTEM is an FDA 510(k)-cleared medical device (K040651) 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 August 9, 2004. Regulation: 8.