Protech Professional Products, Inc. is one of 13028 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Protech Professional Products, Inc. - FDA 510(k) Cleared Devices
Recent clearances: ProTech Plus
2
Total
2
Cleared
0
Denied
Protech Professional Products, Inc. has 2 FDA 510(k) cleared medical devices. Based in Centereach, US.
Historical record: 2 cleared submissions from 1993 to 2015. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Protech Professional Products, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Acdm Consulting, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Protech Professional Products, Inc.
2 devices