Medical Device Manufacturer · US , Ramona , CA

Airpharma, LLC

2 submissions · 2 cleared · Since 1994
2
Total
2
Cleared
0
Denied

Airpharma, LLC — FDA 510(k) Submissions

Airpharma, LLC has submitted 2 FDA 510(k) premarket notifications since 1994, of which 2 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Nebulizer (direct Patient Interface), Nebulizer, Medicinal, Non-ventilatory (atomizer) . Use the specialty filter in the sidebar to narrow results.

2 devices
1–2 of 2
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All2 Anesthesiology 2