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Understanding 21 CFR Part 882: Regulatory Standards for Neurological Devices
21 CFR Part 882 outlines the regulatory requirements set forth by the U.S. Food and Drug Administration (FDA) for neurological devices.
Oct 22, 20243 min read


Elon Musk's Neuralink Secures FDA Approval for Human Trials
Elon Musk's Neuralink has achieved a major milestone with FDA authorization for its first human clinical trials.
Sep 26, 20242 min read


Apple AirPods Pro 2 Gains FDA Clearance for Groundbreaking Move Into the OTC Hearing Aid Market
In a landmark move, Apple has ventured into the healthcare market by positioning the Apple AirPods Pro 2 as over-the-counter hearing aids.
Sep 16, 20244 min read
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