
Senorx, Inc.
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SENOSONIX ULTRASOUND BREAST BIOPSY SYSTEM is an FDA 510(k)-cleared medical device (K072541) manufactured by Senorx, 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 September 24, 2007. Regulation: 8.