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Titles
- Design considerations and pre-market submission recommendations for interoperable medical devices: guidance for industry and Food and Drug Administration staff1
- Electromagnetic compatibility (EMC) of medical devices: guidance for industry and Food and Drug Administration staff1
- FDA should further integrate its review of cybersecurity into the premarket review process for medical devices1
- Pediatric information for x-ray imaging device premarket notifications: guidance for industry and Food and Drug Administration staff1
- Safety in the MR environment: MR safety screening practices1
- Safety in the MR environment: ferromagnetic projectile objects in the MRI scanner room1