SIPHONGUARD CSF CONTROL DEVICE

SIPHONGUARD CSF CONTROL DEVICE is an FDA 510(k)-cleared medical device (K992173) manufactured by Johnson & Johnson Professionals, 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 6, 2000. Regulation: 8.