
Smiths Medical Asd, Inc.
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Hypodermic Needle-Pro® EDGE Safety Device with Low Dead Space Syringe is an FDA 510(k)-cleared medical device (K232943) manufactured by Smiths Medical Asd, Inc.. This device is classified under the General Hospital specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on May 30, 2024. Regulation: 8.

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