
Pajunk GmbH
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PAJUNK TUOHY NEEDLES, QUINCKE NEEDLES, CHIBA NEEDLES & CRAWFORD NEEDLES is an FDA 510(k)-cleared medical device (K040965) 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 September 6, 2004. Regulation: 8.