FDA clears SenoRx US breast biopsy device

AuntMinnie.com staff writers
Oct 18, 2007

Breast cancer interventional device firm SenoRx announced that the U.S. Food and Drug Administration (FDA) has cleared its SenoSonix System.

SenoSonix combines the company's EnCor vacuum-assisted biopsy technology with an ultrasound system developed by Ultrasonix Medical of Richmond, British Columbia.

Ultrasonix has installed more than 1,000 of its Sonix series Smart Ultrasound systems worldwide; SenoRx has an installed base of more than 400 for its breast biopsy systems in the U.S. and Canada, according to the Aliso Viejo, CA-based vendor. The device will be marketed as SenoSonix with EnCore Inside.

By AuntMinnie.com staff writers
October 19, 2007

Related Reading

SenoRx prices IPO, March 30, 2007

Road to RSNA, SenoRx, November 9, 2006

Suros and SenoRx to bury patent hatchet, May 25, 2006

SenoRx adds new probe, February 23, 2006

SenoRx lands patent for partial-breast radiation balloon, January 17, 2006

Copyright © 2007 AuntMinnie.com

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