Urethrotech is one of 195 FDA 510(k) medical device manufacturers from United Kingdom in the dataset, ranked by real submission volume.
Urethrotech - FDA 510(k) Cleared Devices
Recent clearances: Urethrotech UCD
1
Total
1
Cleared
0
Denied
Urethrotech has 1 FDA 510(k) cleared medical devices. Based in Kingston Upon Thames, GB.
Historical record: 1 cleared submissions from 2019 to 2019. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Urethrotech Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Smith Associates as regulatory consultant.
FDA 510(k) Regulatory Record - Urethrotech
1 devices