NITROGLYCERIN I.V. ADMINISTRATION SET

NITROGLYCERIN I.V. ADMINISTRATION SET is an FDA 510(k)-cleared medical device (K833939) manufactured by Critikon Company, LLC. This device is classified under the General Hospital specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on February 20, 1984. Regulation: 8.