VITEK 2 AST-Streptococcus Inducible Clindamycin Resistance

VITEK 2 AST-Streptococcus Inducible Clindamycin Resistance is an FDA 510(k)-cleared medical device (K260282) 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 April 14, 2026. Regulation: 8.