IMMULITE 2000, IMMULITE 2500 VANCOMYCIN

IMMULITE 2000, IMMULITE 2500 VANCOMYCIN is an FDA 510(k)-cleared medical device (K063045) manufactured by Diagnostic Products Corp.. This device is classified under the Clinical Toxicology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on December 4, 2006. Regulation: 8.