MODIFIED AMANA ELECTROTHERAPEUTIC SYSTEM

MODIFIED AMANA ELECTROTHERAPEUTIC SYSTEM is an FDA 510(k)-cleared medical device (K875072) manufactured by Amana Medical Group. This device is classified under the Neurology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on September 21, 1988. Regulation: 8.