Regulatory Management Services is one of 22865 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Regulatory Management Services - FDA 510(k) Cleared Devices
Recent clearances: INTERSON USB ULTRASOUND PROBE SYSTEM, MINI IMAGER, PREVIEW TELEIMAGING SYSTEM
3
Total
3
Cleared
0
Denied
Regulatory Management Services has 3 FDA 510(k) cleared medical devices. Based in San Leandro, US.
Historical record: 3 cleared submissions from 1995 to 2007. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Regulatory Management Services 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 - Regulatory Management Services
3 devices