Final rule 2025-16033
Medical Devices; Radiology Devices; Classification of the Liver Iron Concentration Imaging Companion Diagnostic for Deferasirox
The Food and Drug Administration (FDA, the Agency, or we) is classifying the liver iron concentration imaging companion diagnostic for deferasirox 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 classification of the liver iron concentration imaging companion diagnostic for deferasirox. We are taking this action because we have determined that classifying the device into class II 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.
Source-supplied record
Document details
- Document number
- 2025-16033
- Published
- Aug 21, 2025
- Effective
- Aug 21, 2025
- Comments close
- Not supplied
- Federal Register citation
- 90 FR 40734
Docket identifiers
- Docket No. FDA-2025-N-2369
CFR references
- Title 21, part 892