Curlview Igt, LLC is one of 24542 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Curlview Igt, LLC - FDA 510(k) Cleared Devices
Recent clearances: CARDIO-VIEW
1
Total
1
Cleared
0
Denied
Curlview Igt, LLC has 1 FDA 510(k) cleared medical devices. Based in Newton, US.
Historical record: 1 cleared submissions from 2008 to 2008. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Curlview Igt, LLC 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 - Curlview Igt, LLC
1 devices