Vycor Medical, LLC is one of 24549 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Vycor Medical, LLC - FDA 510(k) Cleared Devices
Recent clearances: VYCOR SURGICAL ACCESS SYSTEMS
1
Total
1
Cleared
0
Denied
Vycor Medical, LLC has 1 FDA 510(k) cleared medical devices. Based in Shelton, US.
Historical record: 1 cleared submissions from 2006 to 2006. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Vycor Medical, LLC Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Tuv Rheinland of North America, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Vycor Medical, LLC
1 devices