ACCUPROBE STREPTOCOCCUS PNEUMONIAE CULTURE CONFIR.

ACCUPROBE STREPTOCOCCUS PNEUMONIAE CULTURE CONFIR. is an FDA 510(k)-cleared medical device (K902908) manufactured by Gen-Probe, Inc.. This device is classified under the Microbiology specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on August 5, 1990. Regulation: 8.