Vycor Medical, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Vycor Medical, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Vycor Medical Viewsite Brain Access System (“VBAS”) and VBAS with Alignment Clip (“VBAS AC”) (together the “VBAS Family”)
1
Total
1
Cleared
0
Denied
Vycor Medical, Inc. has 1 FDA 510(k) cleared medical devices. Based in Boca Raton, US.
Last cleared in 2021. Active since 2021. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Vycor Medical, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Mdi Consultant, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Vycor Medical, Inc.
1 devices