VERIL/PPR PERSONAL PAIN RELIEVER #800

VERIL/PPR PERSONAL PAIN RELIEVER #800 is an FDA 510(k)-cleared medical device (K822929) manufactured by Verite. This device is classified under the Neurology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on November 16, 1982. Regulation: 8.