PHARMASEAL CLEAR HUB SPINAL NEEDLE

PHARMASEAL CLEAR HUB SPINAL NEEDLE is an FDA 510(k)-cleared medical device (K920305) 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 January 26, 1993. Regulation: 8.