Pinpoint GT Needle Guide Kits

Pinpoint GT Needle Guide Kits is an FDA 510(k)-cleared medical device (K171348) manufactured by C.R. Bard, Inc.. This device is classified under the Radiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on May 21, 2017. Regulation: 8.