Vista Lifesciences, Inc. is one of 16396 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Vista Lifesciences, Inc. - FDA 510(k) Cleared Devices
Recent clearances: ANAM Test System, ANAM Test System: Military Battery
2
Total
2
Cleared
0
Denied
Vista Lifesciences, Inc. has 2 FDA 510(k) cleared medical devices. Based in Parker, US.
Last cleared in 2021. Active since 2015. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Vista Lifesciences, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Biologics Consulting Group, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Vista Lifesciences, Inc.
2 devices