BD BACTEC Plus Aerobic/F Culture Vials (plastic)

BD BACTEC Plus Aerobic/F Culture Vials (plastic) is an FDA 510(k)-cleared medical device (K113558) 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 15, 2012. Regulation: 8.