FDA Device Intelligence
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Screen, Intensifying, Radiographic

FDA product code EAM · Class 1 · Radiology

273
Registered devices
0
Adverse events
4
Recalls
35
510(k) clearances

Devices with this code

Recent recalls

DateFirmReason
2004-03-30General Electric Med SystemsThe ball joint that attaches the single monitor platform to the system boom could fail causing the monitor to fall.
2004-03-30General Electric Med SystemsThe ball joint that attaches the single monitor platform to the system boom could fail causing the monitor to fall.
2004-03-30General Electric Med SystemsThe ball joint that attaches the single monitor platform to the system boom could fail causing the monitor to fall.
2004-03-30General Electric Med SystemsThe ball joint that attaches the single monitor platform to the system boom could fail causing the monitor to fall.

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Sourced from public U.S. FDA data. Informational only — not medical or regulatory advice. Not affiliated with the FDA.