ACTH IRMA KIT MITSUBISHI YUKA

ACTH IRMA KIT MITSUBISHI YUKA is an FDA 510(k)-cleared medical device (K910178) manufactured by Science Regulatory Services Intl.. 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 May 21, 1991. Regulation: 8.