Avitro, LLC is one of 26041 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Avitro, LLC - FDA 510(k) Cleared Devices
Recent clearances: 0.9% SODIUM CHLORIDE VASCULAT ACCESS DEVICE, THE AVITRO LLC, 10 AND 100 USO UNITS/ML HEPARIN SODIUM VAFD
2
Total
2
Cleared
0
Denied
Avitro, LLC has 2 FDA 510(k) cleared medical devices. Based in Woodstock, US.
Historical record: 2 cleared submissions from 2000 to 2000. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Avitro, LLC Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Avitro, LLC
2 devices