🩻FDA Classifies Radiological Devices to Enhance Market Access
Medical Devices; Radiology Devices; Classification of the Radiological Acquisition and/or Optimization Guidance System
Summary
The Food and Drug Administration (FDA, the Agency, or we) is classifying the radiological acquisition and/or optimization guidance 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 radiological acquisition and/or optimization guidance 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.
Agencies
- Health and Human Services Department
- Food and Drug Administration
Business Impact
$$ - Med
This regulation classifies the radiological acquisition guidance system as class II, reducing regulatory burdens, which can result in cost savings and faster market entry for businesses. This classification allows companies to use a streamlined 510(k) process for future devices.