CSF-VENTRICULOSTOMY RESERVOIR

CSF-VENTRICULOSTOMY RESERVOIR is an FDA 510(k)-cleared medical device (K874498) manufactured by Pudenz-Schulte Medical Research Corp.. This device is classified under the Neurology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on February 10, 1988. Regulation: 8.