USE OF TWEEN 80 AS A WETTING AGENT ON

USE OF TWEEN 80 AS A WETTING AGENT ON is an FDA 510(k)-cleared medical device (K832802) manufactured by American Bentley. This device is classified under the Cardiovascular specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on December 28, 1983. Regulation: 8.