Trutek, Inc. is one of 25857 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Trutek, Inc. - FDA 510(k) Cleared Devices
Recent clearances: TRUTEK SELECT MODEL TT-1001
1
Total
1
Cleared
0
Denied
Trutek, Inc. has 1 FDA 510(k) cleared medical devices. Based in Crofton, US.
Historical record: 1 cleared submissions from 2003 to 2003. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Trutek, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Entela, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Trutek, Inc.
1 devices