ACUSON TRANSPERINEAL NEEDLE GUIDE

ACUSON TRANSPERINEAL NEEDLE GUIDE is an FDA 510(k)-cleared medical device (K874922) manufactured by Acuson Computed Sonography. This device is classified under the Radiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on February 18, 1988. Regulation: 8.