ATRAUMATIC STANDARD SPROTTE NEEDLE

ATRAUMATIC STANDARD SPROTTE NEEDLE is an FDA 510(k)-cleared medical device (K911202) manufactured by Pajunk GmbH. This device is classified under the Anesthesiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on May 3, 1992. Regulation: 8.