ViroZap Indoor Air Purifier, In Duct Model 1008
Aug 2024
99d
Applied Photonix, LLC
1
Total
1
Cleared
0
Denied
Applied Photonix, LLC — FDA 510(k) Submissions
Applied Photonix, LLC has submitted 1 FDA 510(k) premarket notifications since 2024, of which 1 received clearance as substantially equivalent to a predicate device.
The company's most frequent device categories include Purifier, Air, Ultraviolet, Medical . Use the specialty filter in the sidebar to narrow results.
1 devices