Percuvision, LLC is one of 16101 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Percuvision, LLC - FDA 510(k) Cleared Devices
Recent clearances: DIRECTVISION GUIDE SYSTEM, PERCUCATH URINARY CATHETER
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.
510(k) submissions have been managed by Underwriters Laboratories, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Percuvision, LLC
2 devices