BECKMAN DIATRAC HEMOGLOBIN A ELECTROPHORESIS KIT

BECKMAN DIATRAC HEMOGLOBIN A ELECTROPHORESIS KIT is an FDA 510(k)-cleared medical device (K905709) manufactured by Beckman Instruments, Inc.. 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 22, 1991. Regulation: 8.