RADx Intraoral Appliance for Snoring and Sleep Apnea
Jul 2023
135d
Achaemenid, LLC
1
Total
1
Cleared
0
Denied
Achaemenid, LLC — FDA 510(k) Submissions
Achaemenid, LLC has submitted 1 FDA 510(k) premarket notifications since 2023, of which 1 received clearance as substantially equivalent to a predicate device.
The company's most frequent device categories include Device, Jaw Repositioning . Use the specialty filter in the sidebar to narrow results.
1 devices