FDA Device Intelligence
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Collimator, Manual, Radiographic

FDA product code IZX · Class 2 · Radiology

162
Registered devices
5
Adverse events
4
Recalls
17
510(k) clearances

Devices with this code

Recent recalls

DateFirmReason
2011-10-28Shimadzu Medical SystemsShimadzu is recalling Diagnostic X-ray Beam-Limiting Device, Mobile x-ray system and Diagnostic x-ray tube assembly because they do not comply with the Product
2007-08-10Summit Industries Inc.The D800 Swivel Collimator may come loose from the tubestand and fall onto the x-ray table.
2007-08-10Summit Industries Inc.The E600 Swivel Collimator may come loose from the tubestand and fall onto the x-ray table.
2007-08-10Summit Industries Inc.The F100 Swivel Collimator may come loose from the tubestand and fall onto the x-ray table.

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