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AireHealth Earns FDA 510(k) Clearance for Portable Nebulizer

December 8, 2020

The FDA has granted 510(k) clearance for AireHealth’s connected nebulizer, VitalMed, a device that nebulizes liquid medications for inhalation by patients with respiratory conditions.

The portable electronic device is cleared for use in both home and healthcare settings for patients aged two and above. The chargeable device is lightweight, silent and small in size.

The company said its nebulizer will be able to connect to a new symptom-tracking companion app, VitalCompanion, starting next year.

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