Protom International Holding Corporation is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Protom International Holding Corporation - FDA 510(k) Cleared Devices
Recent clearances: Radiance 330 Proton Beam Therapy System
1
Total
1
Cleared
0
Denied
Protom International Holding Corporation has 1 FDA 510(k) cleared medical devices. Based in Wakefield, US.
Historical record: 1 cleared submissions from 2019 to 2019. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Protom International Holding Corporation Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Hogan Lovells US LLP as regulatory consultant.
FDA 510(k) Regulatory Record - Protom International Holding Corporation
1 devices