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Hommed, LLC
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HOMMED SENTRY III PATIENT MONITOR SYSTEM WITH CARD READER is an FDA 510(k)-cleared medical device (K014025) 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 April 8, 2002. Regulation: 8.