VITEK® 2 Streptococcus Tetracycline (<=0.25 - >=16 µg/mL)

VITEK® 2 Streptococcus Tetracycline (<=0.25 - >=16 µg/mL) is an FDA 510(k)-cleared medical device (K223481) manufactured by bioMerieux, 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 February 2, 2023. Regulation: 8.