P-S MEDICAL CSF-LUMBOPERITONEAL SHUNT

P-S MEDICAL CSF-LUMBOPERITONEAL SHUNT is an FDA 510(k)-cleared medical device (K831396) 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 August 11, 1983. Regulation: 8.