SANTA BARBARA MEDCO-LANTOPHORETIC APPLIC

SANTA BARBARA MEDCO-LANTOPHORETIC APPLIC is an FDA 510(k)-cleared medical device (K842483) manufactured by Santa Barbara Medco, 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 30, 1984. Regulation: 8.