RE-VENT ARTERIAL BLOOD SAMPLER AND/OR BIOSAMPLER

RE-VENT ARTERIAL BLOOD SAMPLER AND/OR BIOSAMPLER is an FDA 510(k)-cleared medical device (K882975) manufactured by Richmann 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 January 24, 1989. Regulation: 8.