Vital Art and Science Incorporated is one of 14057 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Vital Art and Science Incorporated - FDA 510(k) Cleared Devices
Recent clearances: myVision Track Model 005, MYVISIONTRACK(TM)
2
Total
2
Cleared
0
Denied
Vital Art and Science Incorporated has 2 FDA 510(k) cleared medical devices. Based in Richardson, US.
Historical record: 2 cleared submissions from 2013 to 2015. Primary specialty: Ophthalmic.
Browse the FDA 510(k) cleared devices submitted by Vital Art and Science Incorporated Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by O'Connell Regulatory Consultants, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Vital Art and Science Incorporated
2 devices