ACTIVAPATCH ET IONTOPHORESIS PATCH

ACTIVAPATCH ET IONTOPHORESIS PATCH is an FDA 510(k)-cleared medical device (K132832) manufactured by Activatek, 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 February 12, 2014. Regulation: 8.