ACCUPROBE HISTOPLASMA CAPSULATUM CULTURE CONF.TEST

ACCUPROBE HISTOPLASMA CAPSULATUM CULTURE CONF.TEST is an FDA 510(k)-cleared medical device (K896859) manufactured by Gen-Probe, Inc.. This device is classified under the Microbiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on January 31, 1990. Regulation: 8.