Healthcare Industry News: Surgical Ablation
News Release - April 23, 2012
AngioDynamics Resumes NanoKnife(R) System Shipments in the U.S.ALBANY, N.Y., April 23, 2012 -- (Healthcare Sales & Marketing Network) -- AngioDynamics (Nasdaq:ANGO ), a leading provider of innovative, minimally invasive medical devices for vascular access, surgery, peripheral vascular disease and oncology, today announced the resumption of shipments of its NanoKnife(R) System in the U.S. market following a software modification that removed the Ablation Zone Estimator (AZE) feature pursuant to previously announced voluntary actions.
In the United States, NanoKnife has been cleared by the FDA for use in the Surgical Ablation of soft tissue. NanoKnife has not been cleared for the treatment or therapy of a specific disease or condition.
AngioDynamics, Inc. is a leading provider of innovative, minimally invasive medical devices used by professional healthcare providers for vascular access, surgery, peripheral vascular disease and oncology. AngioDynamics' diverse product lines include market-leading ablation systems, vascular access products, angiographic products and accessories, angioplasty products, drainage products, thrombolytic products and venous products. More information is available at www.AngioDynamics.com.
Issuer of this News Release is solely responsible for its
Please address inquiries directly to the issuing company.