PARENCHYMAL BOLT PRESSURE MONITORING KIT

PARENCHYMAL BOLT PRESSURE MONITORING KIT is an FDA 510(k)-cleared medical device (K981846) manufactured by Camino Neurocare, 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 August 17, 1998. Regulation: 8.