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See today's BioWorld MedTech
Home » FDA says changes in Dexcom G6, G7 sensors constitute misbranding
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FDA says changes in Dexcom G6, G7 sensors constitute misbranding

March 26, 2025
By Mark McCarty
The U.S. FDA’s March 4, 2025, warning letter to Dexcom Inc. is a well-detailed but heavily redacted document explaining the agency’s misgivings about procedures such as monitoring of acetaminophen content in glucose test dishes.
BioWorld MedTech Diabetes Continuous glucose monitor (CGM) U.S. CDRH FDA

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