SIEMENS SIRECUST 730, PATIENT MONITOR W/ARRHYTHMIA

SIEMENS SIRECUST 730, PATIENT MONITOR W/ARRHYTHMIA is an FDA 510(k)-cleared medical device (K894460) manufactured by Siemens Medical Electronics. This device is classified under the Cardiovascular specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on October 1, 1989. Regulation: 8.