HYDROCEPHALUS SHUNT SYSTEM, LOW/MEDIUM/HIGH PRESS.

HYDROCEPHALUS SHUNT SYSTEM, LOW/MEDIUM/HIGH PRESS. is an FDA 510(k)-cleared medical device (K895524) manufactured by Theramed, 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 9, 1990. Regulation: 8.