AUTOMATED MULTI-POINT BLOOD VOLUME ANALYZER

AUTOMATED MULTI-POINT BLOOD VOLUME ANALYZER is an FDA 510(k)-cleared medical device (K964406) manufactured by Daxor Corporation. This device is classified under the Hematology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on September 24, 1997. Regulation: 8.