HEPARIN LOCK FLUSH SOLUTION USP KIT

HEPARIN LOCK FLUSH SOLUTION USP KIT is an FDA 510(k)-cleared medical device (K841305) manufactured by Solo Pak Laboratories. 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 June 3, 1984. Regulation: 8.