BD BACTEC™ Plus Aerobic/F Culture Vials

BD BACTEC™ Plus Aerobic/F Culture Vials is an FDA 510(k)-cleared medical device (K222591) manufactured by Becton, Dickinson and Company. This device is classified under the Microbiology specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on March 23, 2023. Regulation: 8.