MODIFIED ICT/B INTRACRANIAL PRESS. TRANS. EPIDURAL

MODIFIED ICT/B INTRACRANIAL PRESS. TRANS. EPIDURAL is an FDA 510(k)-cleared medical device (K863479) manufactured by Medical Measurements, 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 October 13, 1986. Regulation: 8.