PREZAPAK L ARTERIAL BLOOD SAMPLING KIT

PREZAPAK L ARTERIAL BLOOD SAMPLING KIT is an FDA 510(k)-cleared medical device (K801015) manufactured by Kimble-Terumo, Inc.. This device is classified under the Clinical Chemistry specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on May 13, 1980. Regulation: 8.