GRAHAM-FIELD SALINE ELECTROLYTE GEL

GRAHAM-FIELD SALINE ELECTROLYTE GEL is an FDA 510(k)-cleared medical device (K944600) manufactured by Chester Labs, Inc.. This device is classified under the Neurology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on November 19, 1995. Regulation: 8.