Neuro-Eye Diagnostic Systems, LLC - FDA 510(k) Cleared Devices

Neuro-Eye Diagnostic Systems, LLC has 1 FDA 510(k) cleared medical devices. Based in Houston, US.

Last cleared in 2022. Active since 2022. Primary specialty: Ophthalmic.

Browse the FDA 510(k) cleared devices submitted by Neuro-Eye Diagnostic Systems, LLC Filter by specialty or product code using the sidebar.

510(k) submissions have been managed by Proxima Clinical Research, Inc. as regulatory consultant. 1 device has linked clinical trial registered on ClinicalTrials.gov.