We use cookies to provide you with a better experience. By continuing to browse the site you are agreeing to our use of cookies in accordance with our Cookie Policy.
State Health Commissioner Fred Jacobs said yesterday hospitals will soon be required to submit reports on single-use medical devices that are being reprocessed and then used again on patients, rather than thrown away.
The Neurological Devices Panel of the Medical Devices Advisory Committee will meet Oct. 31 to discuss and make recommendations on a premarket notification application for a depression disorder device and discuss study reports for two recently approved neurological device premarket approval applications.
True mobility in medical products is a wish, not a reality, says Rex Bare, president of Omnica Corporation, the Irvine, California firm that developed two breakthrough oxygen devices that enable people to move about freely for extended periods of time.
Boston Scientific Corporation announced the U.S. market launch of the FLEXView System for unilateral visualization and routing in microwave cardiac surgical ablation procedures.
St. Jude Medical, Inc. announced U.S. Food and Drug Administration (FDA) and European CE Mark approvals of the new Tendril(R) ST model 1788 lead, a new pacemaker lead whose thin structure is designed for easier implantation.
Pivotal Corporation, a leading Customer Relationship Management (CRM) solution provider and the CRM division of CDC Software, the enterprise software company of CDC Corporation announced that medical device manufacturer Lake Region Manufacturing is using Pivotal CRM to help deliver superior customer service and drive significant cost-savings throughout their business.