Federal Register: FDA Action Eases Approval Process for Devices Protecting Esophagus During Cardiac Ablation
September 10, 2026
September 10, 2026
WASHINGTON, Sept. 10 (TNSFR) -- The U.S. Department of Health and Human Services Food and Drug Administration issued the following action in the Federal Register.
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Medical Devices; Cardiovascular Devices; Classification of the Mechanical Deviation Device for Esophageal Protection During Cardiac Ablation Procedures
The Food and Drug Administration (FDA) is classifying the mechanical deviation device for esophageal protection during cardiac ablation proc . . .
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Medical Devices; Cardiovascular Devices; Classification of the Mechanical Deviation Device for Esophageal Protection During Cardiac Ablation Procedures
The Food and Drug Administration (FDA) is classifying the mechanical deviation device for esophageal protection during cardiac ablation proc . . .