HOLGRATH PLASTIC-HUB, QUINCKE SPINAL NEEDLE

HOLGRATH PLASTIC-HUB, QUINCKE SPINAL NEEDLE is an FDA 510(k)-cleared medical device (K944907) manufactured by Holgrath Medical Technologies, Inc.. This device is classified under the Anesthesiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on June 6, 1995. Regulation: 8.