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Surgical Theater's Surgical Navigation Advanced Platform Receives FDA Clearance
2014-06-30 06:00:00| Industrial Newsroom - All News for Today
Technology provides surgeons with advanced imaging and augmented reality capabilities in the operating room<br /> <br /> CLEVELAND – Surgical Theater, LLC today received Food and Drug Administration (FDA) clearance on the recently launched Surgical Navigation Advanced Platform (SNAP). The SNAP integrates with operating room technology to provide advanced 3D capabilities and augmented reality, allowing surgeons to enhance their surgery performance and "see what can't be seen." <br /> <br ...This story is related to the following:Medical & Health Care Software | Communications Software | Software
Tags: advanced
navigation
platform
clearance
Edwards Receives FDA Clearance for Advanced Noninvasive Monitoring System
2014-06-30 06:00:00| Industrial Newsroom - All News for Today
ClearSight system enables clinicians to reduce risk of post-surgical complications<br /> <br /> IRVINE, CA — Edwards Lifesciences Corporation (NYSE: EW), the global leader in the science of heart valves and hemodynamic monitoring, today announced it has received U.S. Food and Drug Administration (FDA) clearance for the ClearSight system.<br /> <br /> The ClearSight system is a noninvasive monitor that provides clinicians access to valuable blood volume and blood flow information for ...This story is related to the following:Sensors, Monitors and Transducers Sponsored by: BEI Sensors (BEI Industrial Encoders) - Cat Sponsor Jan 2014 Search for suppliers of: Blood Pressure Monitors
Tags: system
advanced
monitoring
clearance
India's Ranbaxy gets FDA approval for Novartis's Diovan generic
2014-06-27 10:50:23| Chemicals - Topix.net
India's Ranbaxy Laboratories Ltd has received approval from the U.S. Food and Drug Administration to launch a cheaper copy of Novartis AG's blood pressure pill Diovan, bolstering its outlook after a raft of regulatory bans for poor production quality at its India facilities dented investor sentiment.
Tags: approval
generic
fda
indias
FDA Accepts Mercks NDA for Fixed-Dose Combination of Raltegravir with Lamivudine
2014-06-24 14:30:35| Merck.com - Research & Development News
Dateline City: WHITEHOUSE STATION, N.J. If Approved, Fixed-Dose Combination Would Be Used with Other Antiretroviral Agents for the Treatment of HIV-1 in Adults, Adolescents and Certain Pediatric Patients Merck (NYSE: MRK), known as MSD outside the United States and Canada, today announced that the New Drug Application (NDA) for a fixed-dose combination (FDC) of raltegravir with lamivudine for the treatment of HIV-1 infection (MK-0518B) has been accepted for standard review by the U.S. Food and Drug Administration (FDA). Language: English read more
Tags: with
combination
accepts
fda
FDA approves Cubist antibiotic for skin infections
2014-06-21 01:14:38| Biotech - Topix.net
Regulators cleared the company's Sivextro as a pill and as an intravenous solution for adults with skin infections caused by bacteria that are often resistant to older antibiotics.
Tags: skin
infections
fda
approves
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