IMMULITE/IMMULITE 1000 TURBO INTACT PTH

IMMULITE/IMMULITE 1000 TURBO INTACT PTH is an FDA 510(k)-cleared medical device (K053533) manufactured by Diagnostic Products Corporation. 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 February 2, 2006. Regulation: 8.