Respinova Wins FDA OK for Airway Opening System Pulsehaler

Respinova Wins FDA OK for Airway Opening System Pulsehaler

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Respinova Wins FDA OK for Airway Opening System Pulsehaler

Respinova’s new airway device, called Pulsehaler, has received 510(k) clearance from the U.S. Food and Drug Administration (FDA). That means it can be marketed as a safe and effective medical device to ease breathing in people with airway restrictions, such as chronic obstructive pulmonary disease (COPD). “We are excited to bring this innovative technology to respiratory patients,” Cliff Ansel, CEO of Respinova, said in a press release. “This FDA clearance for Pulsehaler is an important…

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