
C. R. Bard
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Site~Rite 8 Ultrasound System with Cue Needle Tracking System and Pinpoint GT Needle Tech is an FDA 510(k)-cleared medical device (K182281) manufactured by C. R. Bard. This device is classified under the Radiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on October 23, 2018. Regulation: 8.

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