JOHNSON & JOHNSON OPAQUE COLOR MODIFI

JOHNSON & JOHNSON OPAQUE COLOR MODIFI is an FDA 510(k)-cleared medical device (K830491) manufactured by Johnson & Johnson Professionals, 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 March 16, 1983. Regulation: 8.