FDA Device Intelligence
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Processor, Radiographic-Film, Automatic

FDA product code IXW · Class 2 · Radiology

11
Registered devices
45
Adverse events
1
Recalls
83
510(k) clearances

Devices with this code

Recent recalls

DateFirmReason
2016-04-01Fujifilm Medical Systems U.S.A., Inc.Reports of failure of the device's power supply.

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