SD PLUS PATIENT CAT.#78-8010

SD PLUS PATIENT CAT.#78-8010 is an FDA 510(k)-cleared medical device (K840963) manufactured by Codman & Shurtleff, 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 April 22, 1984. Regulation: 8.