MODIFIED USE FOR MODEL 6110A IONTOPHORETIC APPLI.

MODIFIED USE FOR MODEL 6110A IONTOPHORETIC APPLI. is an FDA 510(k)-cleared medical device (K871869) manufactured by Life-Tech Intl., Inc.. This device is classified under the Physical Medicine specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on August 10, 1987. Regulation: 8.