HYBRID NERVE LOCATION NEEDLE COATED AND UNCOATED

HYBRID NERVE LOCATION NEEDLE COATED AND UNCOATED is an FDA 510(k)-cleared medical device (K080603) manufactured by Te ME NA Sas. 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 4, 2008. Regulation: 8.