Vista Ophthalmics, LLC - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Vista Ophthalmics, LLC has 1 FDA 510(k) cleared medical devices. Based in Katy, US.
Last cleared in 2022. Active since 2022. Primary specialty: Ophthalmic.
Browse the FDA 510(k) cleared devices submitted by Vista Ophthalmics, LLC Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Regulatory Pathways Group, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Vista Ophthalmics, LLC
1 devices