BAXTER DISPOSABLE INTRAOSSEOUS INFUSION NEEDLE

BAXTER DISPOSABLE INTRAOSSEOUS INFUSION NEEDLE is an FDA 510(k)-cleared medical device (K930217) manufactured by Baxter Healthcare Corp. 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 February 27, 1994. Regulation: 8.