Business · 17/04/2009Updated: 10/17/2026 · 1 min read

FDA Announces Draft Guidance for Retinal Prostheses IDE Application

The Food and Drug Administration (FDA) has released a draft guidance document outlining recommendations for the development of pre-clinical and clinical tests for retinal prosthetic devices, which must be submitted to the FDA as part of an Investigational Device Exemption (IDE) application.