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FDA Maintains Focus On "Intended Use" For Software-Enabled M
FDA Maintains Focus On "Intended Use" For Software-Enabled M
FDA Maintains Focus On "Intended Use" For Software-Enabled Medical Devices
On June 21, 2023, the U.S. Food and Drug Administration issued a warning letter to Zyto Technologies, Inc. , citing Zyto's promotion of its Hand Cradle Galvanic Skin Response device and associated...
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