PubMed Literature
Medical device publications from PubMed / NCBI
US Food and Drug Administration Clearance of Moderate-Risk Otolaryngologic Devices via the 510(k) Process, 1997-2016.
Read More →Bench-to-bedside: Bridge-enhanced anterior cruciate ligament repair.
Read More →Development of evaluation methods for the approval and review of Intense pulsed light (IPL).
Read More →The Traumatic Brain Injury Endpoints Development (TED) Initiative: Progress on a Public-Private Regulatory Collaboration To Accelerate Diagnosis and Treatment of Traumatic Brain Injury.
Read More →Use of endpoint adjudication to improve the quality and validity of endpoint assessment for medical device development and post marketing evaluation: Rationale and best practices. A report from the cardiac safety research consortium.
Read More →The Long and Winding Road After FDA Approval: A Medical Device Industry Perspective.
Read More →Current State of the Regulatory Trajectory for Whole Slide Imaging Devices in the USA.
Read More →A NEW HEALTH TECHNOLOGY ASSESSMENT SYSTEM FOR DEVICES: THE FIRST FIVE YEARS.
Read More →Incremental Revisions across the Life Span of Ophthalmic Devices after Initial Food and Drug Administration Premarket Approval, 1979-2015.
Read More →Overview of high-risk medical device recalls in obstetrics and gynecology from 2002 through 2016: implications for device safety.
Read More →Risk management and regulations for lower limb medical exoskeletons: a review.
Read More →No matching articles.
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