ECA GEL PROUDUCT REFORMULATION

ECA GEL PROUDUCT REFORMULATION is an FDA 510(k)-cleared medical device (K802647) manufactured by Vanaray Laboratories, 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 January 7, 1981. Regulation: 8.