ROSENTHAL-FRENCH NEBULIZATION DOSIMETER

ROSENTHAL-FRENCH NEBULIZATION DOSIMETER is an FDA 510(k)-cleared medical device (K860800) manufactured by Laboratory For Applied Immunology, Inc.. This device is classified under the Anesthesiology specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on March 26, 1986. Regulation: 8.