NAS receives 510(k) for ClearPath

AuntMinnie.com staff writers

Nov 13, 2006

Radiation therapy products developer North American Scientific (NAS) said it has received 510(k) clearance from the U.S Food and Drug Administration to market the high-dose-rate radiation treatment design of ClearPath, a multicatheter breast brachytherapy device.

ClearPath is placed through a single incision and is designed to conform to the resection cavity following lumpectomy, allowing for more conformal radiation dose distribution during treatment. It also is intended to accommodate either high- or low-dose-rate treatments.

The Chatsworth, CA-based company received 510(k) clearance from the FDA to market the low-dose-rate version of the product, ClearPath CR, in April this year.

By AuntMinnie.com staff writers
November 14, 2006

Related Reading

North American Scientific unveils ClearPath, November 8, 2006

Cutrer to step down as NAS president/CEO, November 3, 2006

NAS gets nomosSTAT install, October 19, 2006

Losses rise, revenues down in NAS' Q3, September 8, 2006

NAS nets FDA nod, July 25, 2006

Copyright © 2006 AuntMinnie.com

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