HAEMOPHILUS TEST MEDIUM (AGAR)

HAEMOPHILUS TEST MEDIUM (AGAR) is an FDA 510(k)-cleared medical device (K892928) manufactured by Remel Co.. This device is classified under the Microbiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on June 12, 1989. Regulation: 8.