IL 301 PORTABLE TRANSCUT. OXYGEN MONI

IL 301 PORTABLE TRANSCUT. OXYGEN MONI is an FDA 510(k)-cleared medical device (K834057) manufactured by Instrumentation Laboratory CO. This device is classified under the Anesthesiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on February 3, 1984. Regulation: 8.