Portal, Inc. is one of 25339 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Portal, Inc. - FDA 510(k) Cleared Devices
Recent clearances: PORTAL GRAVITY SYSTEM
1
Total
1
Cleared
0
Denied
Portal, Inc. has 1 FDA 510(k) cleared medical devices. Based in Logan, US.
Historical record: 1 cleared submissions from 2005 to 2005. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Portal, 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 - Portal, Inc.
1 devices