VITALMAX 800 NON-INVASIVE VITAL SIGN MONITOR/PULSE

VITALMAX 800 NON-INVASIVE VITAL SIGN MONITOR/PULSE is an FDA 510(k)-cleared medical device (K900451) manufactured by Pace Tech, 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 July 17, 1990. Regulation: 8.