SOLACE POST-OPERATIVE PAIN RELIEF INFUSION SYSTEM

SOLACE POST-OPERATIVE PAIN RELIEF INFUSION SYSTEM is an FDA 510(k)-cleared medical device (K060933) manufactured by Apex Medical Technologies, Inc.. This device is classified under the General Hospital specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on May 8, 2006. Regulation: 8.