Request that the FDA take the administrative action to implement minimum RF safety national requirements for MRI devices to increase end-user understanding of the physical locations of RF risks (to better understand and manage those risks) and / or to eliminate the risk of near-field RF burns for MRI patients
🏛 Food and Drug Administration (FDA)FDA-2026-P-6403
Documents
2
Total comments
16
all analyzed
Comment status
Open
Last activity
Jun 19, 2026
In this docket
Documents
Rules, notices, and supporting material — the primary rule pinned first.
- Other· Jun 5, 2026No comment period💬 16
