SIEMENS SIRECUST 700 BEDSIDES/ACCESSORIES, MODIFI

SIEMENS SIRECUST 700 BEDSIDES/ACCESSORIES, MODIFI is an FDA 510(k)-cleared medical device (K921930) 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 May 6, 1993. Regulation: 8.