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Pulmonx Gains Regulatory Approval for Expanded Labeling for Emphysema Treatment

  • Posted by Jenna Widdison
  • On August 1, 2018
Pulmonx Gains Regulatory Approval for Expanded Labeling for Emphysema Treatment New labeling clears the way for the treatment of many more patients. January 10, 2012, Neuchâtel, Switzerland – Pulmonx SARL today announced that its European notified body has granted CE approval for expanded labeling of its Zephyr® endobronchial valve (EBV). The approval was based upon an...
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Pulmonx Reports New Publication Confirms Efficacy of Emphysema Treatment

  • Posted by Jenna Widdison
  • On August 1, 2018
Zephyr® Endobronchial Valve (EBV) therapy guided by Chartis®Assessment is effective in a broad range of patients. May 10, 2012 ,Peseux, Switzerland, Pulmonx, an emerging leader in interventional pulmonology, announced today that the European Respiratory Journal has published the results of the...
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Pulmonx Gets FDA Nod for U.S. Trial of Emphysema Therapy

  • Posted by Jenna Widdison
  • On August 1, 2018
IDE for Study of Zephyr® Endobronchial Valve Approved August 27, 2012, Redwood City, CA, USA - Pulmonx, an emerging leader in interventional pulmonology, announced today that the U.S. Food and Drug Administration (FDA) has approved its request for an Investigational Device Exemption (IDE) to...
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Pulmonx Gets FDA Nod for U.S. Trial of Emphysema Therapy

  • Posted by Chris Kellett
  • On August 27, 2012
August 27, 2012, Redwood City, CA, USA - Pulmonx, an emerging leader in interventional pulmonology, announced today that the U.S. Food and Drug Administration (FDA) has approved its request for an Investigational Device Exemption (IDE) to commence a multi-center pivotal clinical trial.
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Pulmonx Gains Regulatory Approval for Expanded Labeling for Emphysema Treatment

  • Posted by Chris Kellett
  • On January 10, 2012
January 10, 2012, Neuchâtel, Switzerland – Pulmonx SARL today announced that its European notified body has granted CE approval for expanded labeling of its Zephyr® endobronchial valve (EBV). The approval was based upon an independent review of clinical data from numerous studies including the recently completed Chartis multi-center study1 and the European VENT study (a randomized multi-center European trial of Zephyr EBV therapy)2.
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