MODIFICATION TO VSM- VITAL SIGNS MONITOR, (VSM 300 )

MODIFICATION TO VSM- VITAL SIGNS MONITOR, (VSM 300 ) is an FDA 510(k)-cleared medical device (K063419) manufactured by Welch Allyn Protocol, 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 December 3, 2006. Regulation: 8.