SHEER GLYDE DAMS

SHEER GLYDE DAMS is an FDA 510(k)-cleared medical device (K990067) manufactured by Louise C. Myers. This device is classified under the Obstetrics/Gynecology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on February 18, 1999. Regulation: 8.