LISS BODY STIMULATOR MODEL SBL501-M

LISS BODY STIMULATOR MODEL SBL501-M is an FDA 510(k)-cleared medical device (K896226) manufactured by Medical Consultants Intl. , Ltd.. This device is classified under the Neurology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on April 9, 1990. Regulation: 8.