AireHealth Announces FDA 510(k) Clearance of Connected Nebulizer for Patients with Respiratory Conditions
AireHealth, an innovative digital health company empowering and improving healthy living through affordable treatments, symptom tracking and early detection of respiratory conditions, today announced it received 510(k) clearance from the U.S. Food and Drug Administration (FDA) for its connected nebulizer.
- AireHealth, an innovative digital health company empowering and improving healthy living through affordable treatments, symptom tracking and early detection of respiratory conditions, today announced it received 510(k) clearance from the U.S. Food and Drug Administration (FDA) for its connected nebulizer.
- In 2021, AireHealth will also add VitalCapacity , a connected spirometer, to its VitalBreath respiratory care platform.
- AireHealth is pleased to have received 510(k) clearance of our connected nebulizer from the FDA, which will support the creation of an overall ecosystem of connected solutions to treat patients with respiratory conditions.
- The acquisition has positioned AireHealth to integrate data collection and analysis capabilities into its connected respiratory care platform.