DISPERSALLOY-DISPERSED PHASE ALLOY SELF-

DISPERSALLOY-DISPERSED PHASE ALLOY SELF- is an FDA 510(k)-cleared medical device (K802967) manufactured by Johnson & Johnson Professionals, Inc.. This device is classified under the Dental specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on December 29, 1980. Regulation: 8.