SMARTMIST ASTHMA MANAGMENT SYSTEM, SMARTMIST, MODEL NUMBER SM-100/SMARTMIST SPIROMETRY AIRWAY, MODEL NUMBER SA-100
May 1996
88d
Aradigm Corp.
1
Total
1
Cleared
0
Denied
Aradigm Corp. — FDA 510(k) Submissions
Aradigm Corp. has submitted 1 FDA 510(k) premarket notifications since 1996, of which 1 received clearance as substantially equivalent to a predicate device.
The company's most frequent device categories include Nebulizer, Medicinal, Non-ventilatory (atomizer) . Use the specialty filter in the sidebar to narrow results.
1 devices