AP-4000, AIR PULSE SENSORY STIMULATOR

AP-4000, AIR PULSE SENSORY STIMULATOR is an FDA 510(k)-cleared medical device (K964815) manufactured by Pentax Precision Instrument Corp.. This device is classified under the Neurology specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on September 3, 1997. Regulation: 8.