CLEAR HUB SPINAL NEEDLE, 18, 20, 22, 25 GA.

CLEAR HUB SPINAL NEEDLE, 18, 20, 22, 25 GA. is an FDA 510(k)-cleared medical device (K951949) manufactured by Baxter Healthcare Corp. This device is classified under the Anesthesiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on August 10, 1995. Regulation: 8.