CROWN, ACRYLIC, CORAL BRAND, PREFORMED

CROWN, ACRYLIC, CORAL BRAND, PREFORMED is an FDA 510(k)-cleared medical device (K770684) manufactured by Parker Laboratories, Inc.. This device is classified under the Dental specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on April 25, 1977. Regulation: 8.