Percuvision, LLC is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Percuvision, LLC - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
Denied
Percuvision, LLC has 2 FDA 510(k) cleared medical devices. Based in Gahanna, US.
Historical record: 2 cleared submissions from 2009 to 2009. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Percuvision, LLC Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Percuvision, LLC
2 devices