LIFESCOPE 12, BSM 8500A PATIENT MONITOR

LIFESCOPE 12, BSM 8500A PATIENT MONITOR is an FDA 510(k)-cleared medical device (K872241) manufactured by Nihon Kohden America, 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 September 29, 1987. Regulation: 8.