Dualams, Inc., Dba Airkor is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Dualams, Inc., Dba Airkor - FDA 510(k) Cleared Devices
Recent clearances: UltraEzAir® (UEA1A)
1
Total
1
Cleared
0
Denied
Dualams, Inc., Dba Airkor has 1 FDA 510(k) cleared medical devices. Based in Dallas, US.
Latest FDA clearance: Oct 2024. Active since 2024. Primary specialty: Anesthesiology.
Browse the FDA 510(k) cleared devices submitted by Dualams, Inc., Dba Airkor Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by AlvaMed, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Dualams, Inc., Dba Airkor
1 devices