
Becton, Dickinson and Company
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BD Preset and BD A-Line Arterial Blood Collection Syringes is an FDA 510(k)-cleared medical device (K260128) manufactured by Becton, Dickinson and Company. This device is classified under the Clinical Chemistry specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on April 14, 2026. Regulation: 8.