Uberlube, LLC is one of 18443 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
1
Total
1
Cleared
0
Denied
Uberlube, LLC has 1 FDA 510(k) cleared medical devices. Based in Evanston, US.
Historical record: 1 cleared submissions from 2015 to 2015. Primary specialty: Obstetrics & Gynecology.
Browse the FDA 510(k) cleared devices submitted by Uberlube, LLC Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Spectramedex, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Uberlube, LLC
1 devices