
Becton, Dickinson and Company
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BD MAX Enteric Viral Panel is an FDA 510(k)-cleared medical device (K220607) manufactured by Becton, Dickinson and Company. This device is classified under the Microbiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on September 20, 2022. Regulation: 8.

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