Home » RESPIRONICS RECEIVES 510(K) CLEARANCE FROM FDA FOR I-NEB AAD SYSTEM
RESPIRONICS RECEIVES 510(K) CLEARANCE FROM FDA FOR I-NEB AAD SYSTEM
Respironics recently announced the U.S. Food and Drug Administration granted 510(k) clearance of the I-neb Adaptive Aerosol Delivery (AAD) System for the aerosolization of liquid medication approved for use with the I-neb AAD System. The device is cleared for use by the patient in the home care, nursing home, sub-acute institution, or hospital environment.
Yahoo News
KEYWORDS FDAnews Device Daily Bulletin
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