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In Veritas Medical Diagnostics, a firm that designs and develops testing devices, Aug. 17 announced it has filed a patent for a low-cost diagnostic technology that could be used to detect a range of diseases and conditions.
The Government Accountability Office (GAO) said in a study published in July that closures of mammography facilities are outpacing openings of new facilities.
The FDA posted guidance on how device firms can qualify for small business user fee discounts and waivers for agency reviews of their products under the Medical Device User Fee and Modernization Act in fiscal 2007.
Abbott announced
Aug. 15 the enrollment of the first patient in its SPIRIT IV clinical trial for the continued evaluation of the safety and efficacy of the XIENCE(TM) V Everolimus Eluting Coronary Stent System for the treatment of coronary artery disease in a more complex patient population.
Medical device maker BioSphere Medical Inc. has received U.S. Food and Drug Administration approval for a catheter to treat uterine fibroids and vascular tumors.
Solos Endoscopy, Inc. is pleased to announce that the Company is filing with the FDA the documents requesting immediate market clearance on the recently acquired MastaScope and OvaScope product lines.