MILLENNIUM EDITION 2000 ACCELERATED ELECTROFORMING SYSTEM

MILLENNIUM EDITION 2000 ACCELERATED ELECTROFORMING SYSTEM is an FDA 510(k)-cleared medical device (K002675) manufactured by Product Development Industries, Inc.. This device is classified under the Dental specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on October 24, 2000. Regulation: 8.