Veritract, Inc. is one of 15083 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Veritract, Inc. - FDA 510(k) Cleared Devices
Recent clearances: VERITRACT ENTERAL FEEDING TUBE SYSTEM
1
Total
1
Cleared
0
Denied
Veritract, Inc. has 1 FDA 510(k) cleared medical devices. Based in Salt Lake City, US.
Historical record: 1 cleared submissions from 2014 to 2014. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Veritract, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Regulatory Technology Services, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Veritract, Inc.
1 devices