ADVIA CENTAUR FT4, ADVIA CENTAUR T4

ADVIA CENTAUR FT4, ADVIA CENTAUR T4 is an FDA 510(k)-cleared medical device (K132249) manufactured by Siemens Healthcare Diagnostics, Inc.. This device is classified under the Clinical Chemistry specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on September 12, 2013. Regulation: 8.