New Cos Inc. Dba Visionair Solutions is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
New Cos Inc. Dba Visionair Solutions - FDA 510(k) Cleared Devices
Recent clearances: VisionAir Patient-Specific Airway Stent
1
Total
1
Cleared
0
Denied
New Cos Inc. Dba Visionair Solutions has 1 FDA 510(k) cleared medical devices. Based in Cleveland, US.
Last cleared in 2022. Active since 2022. Primary specialty: Anesthesiology.
Browse the FDA 510(k) cleared devices submitted by New Cos Inc. Dba Visionair Solutions Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - New Cos Inc. Dba Visionair Solutions
1 devices