ZapStim Controller Application (Z1023)

ZapStim Controller Application (Z1023) is an FDA 510(k)-cleared medical device (K233631) manufactured by Revital Lab, 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 February 8, 2024. Regulation: 8.