Inspired Technologies Obtains FDA 510(k) Approval for the VIAspire(TM) Liquefier

NORTH HUNTINGDON, Pa.--(BUSINESS WIRE)--Inspired Technologies, Inc., an innovative respiratory device company, today announced it has obtained FDA 510(k) approval for its VIAspire™ Liquefier. The VIAspire Liquefier makes liquid oxygen in the home for patients requiring oxygen therapy, such as those with Chronic Obstructive Pulmonary Disease (COPD). “Oxygen providers no longer have to choose between patient care and operational excellence. We deliver both,” said Dan Easley, President and CEO of Inspired Technologies. “The entire VIAspire Personal Oxygen System will give patients the freedom and confidence to lead more active lives. It also enables our provider network to focus on superior patient results, while strengthening their business model.”

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