CURITY PARACERVICAL/PUDENDAL BLOCK ANES

CURITY PARACERVICAL/PUDENDAL BLOCK ANES is an FDA 510(k)-cleared medical device (K801724) manufactured by The Kendal Co.. 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 6, 1980. Regulation: 8.