CARDIOPHONICS 1000 MEMORY MONITOR

CARDIOPHONICS 1000 MEMORY MONITOR is an FDA 510(k)-cleared medical device (K992772) manufactured by Rlt Medical Assoc., 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 16, 1999. Regulation: 8.