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Medical Devices; Clinical Chemistry and Clinical Toxicology Devices; Classification of the Voriconazole Test System

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The Food and Drug Administration (FDA, Agency, or we) is classifying the voriconazole test system into class II (special controls). The special controls that apply to the device type are identified in this order and will be part of the codified language for the voriconazole test system's classification. We are taking this action because we have determined that classifying the device into class II (special controls) will provide a reasonable assurance of safety and effectiveness of the device. We believe this action will also enhance patients' access to beneficial innovative devices, in part by reducing regulatory burdens.

No lobbying positions or financial data recorded for this regulation yet.

Public comment data and advocacy positions are added as they become available.