Rx Medicare

Diagnostic HYBRIDS announced that the US Food and Drug Administration has cleared an additional claim for the company’s D3 UltraTM DFA Respiratory Virus Identification Kit, which confirms that the assay can detect the 2009 influenza A (H1N1)v virus.

Read More…

Related Posts

• Diagnostic Hybrids Receives FDA Emergency Use Authorization For D3 Ultra 2009 H1N1 Influenza A Virus ID Kit
• Diagnostic Hybrids Announces FDA Clearance Of D3(R) FastPointTM L-DFATM RSV/MPV Identification Kit
• Meridian Granted Special 510(k) Clearance To Add 2009 H1N1 Influenza A Virus Analytical Sensitivity Claim To The TRU FLU(R) Test Package Insert
• PositiveID Corporation Successfully Completes Phase I Development Of Its Rapid Virus Detection System
• FDA Approves Additional Vaccine For 2009 H1N1 Influenza Virus
• USDA Conducting Confirmatory Testing On Possible Detection Of 2009 Pandemic H1N1 Influenza In U.S. Swine
• Warnex Launches Test For Influenza A H1N1 Virus Mutation Associated With Resistance To Tamiflu(R)
• Cases Of The 2009 H1N1 Influenza A Virus Confirmed In Crawford And Miami Counties
• The Immune Response To Influenza Virus Isn’t ‘All Good’
• Development Of Rapid Approach To Identify Influenza A Virus Mutations And Drug Resistance
• USC Researchers Uncover Mechanism That Allows Influenza Virus To Evade The Body¹s Immune Response
• Alertan, circula virus de influenza jamás visto
• EFPIA Response To The A (H1N1) Novel Influenza Virus
• Attacking influenza: how human monoclonal antibodies neutralize the flu virus
• Drug Resistant Influenza A Virus Potentially Serious To High-Risk Patients

Tags: clearance, detection, diagnostic, efficacy, gets, h1n1v, hybrids, influenza, virus

This entry was posted on Wednesday, September 2nd, 2009 at 1:09 am and is filed under Uncategorized. You can follow any responses to this entry through the RSS 2.0 feed. Both comments and pings are currently closed.