- Description
- Uses
- Risks/Benefits
- Information for Patients
- Information for Professionals
- Laws, Regulations Performance Standards
- Industry Guidance
- Other Resources
Download the Poster:
8.5″ x 11″
(4.9 MB) 11″ x 14″
(6.6 MB) 20″ x 30″
(19.8 MB)
Information for Patients
- RadiologyInfo: The Radiology Information Resource for Patients
- FDA’s Radiation-Emitting Products
Information for Patients
- RadiologyInfo: The Radiology Information Resource for Patients
- FDA’s Radiation-Emitting Products
Information for Professionals
- MRI Safety
- FDA Public Health Advisory: Update on Magnetic Resonance Imaging (MRI) Contrast Agents Containing Gadolinium and Nephrogenic Fibrosing Dermopathy
- FDA Public Health Notification: MRI-Caused Injuries in Patients with Implanted Neurological Stimulators
- FDA Public Health Advisory: Risk of Burns during MRI Scans from Transdermal Drug Patches with Metallic Backings
- Cables and electrodes can burn patients during MRI
Federal Food, Drug and Cosmetic Act (FFDCA), Chapter V, Subchapter C – Electronic Product Radiation Control.
Manufacturers of diagnostic x-ray products are responsible for compliance with all applicable requirements of Title 21 Code of Federal Regulations (Subchapter J, Radiological Health) Parts 1000 through 1005:
1003 – Notification of defects or failure to comply
1004 – Repurchase, repairs, or replacement of electronic products
1005 – Importation of electronic products