SYSTEM SIRECUST 400 SIEMENS SIRECUST 456-1A

SYSTEM SIRECUST 400 SIEMENS SIRECUST 456-1A is an FDA 510(k)-cleared medical device (K844791) manufactured by Analogic Corp.. This device is classified under the Cardiovascular specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on April 9, 1985. Regulation: 8.