SIREDOC 60 AND SIREDOC 220

SIREDOC 60 AND SIREDOC 220 is an FDA 510(k)-cleared medical device (K863331) manufactured by Siemens Medical Solutions USA, Inc.. This device is classified under the Cardiovascular specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on October 5, 1986. Regulation: 8.