Home › Device types › IZW
Collimator, Automatic, Radiographic
FDA product code IZW · Class 2 · Radiology
68
Registered devices
9
Adverse events
3
Recalls
23
510(k) clearances
Devices with this code
Claymount — Varex Imaging Nederland B.V.Varex Imaging — Varex Imaging Nederland B.V.Ralco srl — RALCO SRLLINEAR IV — CARESTREAM HEALTH, INC.R-300 — SHIMADZU CORPORATIONRalco srl — RALCO SRLClaymount — Varex Imaging Nederland B.V.Varex Imaging — Varex Imaging Nederland B.V.Claymount — Varex Imaging Nederland B.V.Claymount — Varex Imaging Nederland B.V.Ralco srl — RALCO SRLVarex Imaging — Varex Imaging Nederland B.V.Varex Imaging — Varex Imaging Nederland B.V.Varex Imaging — Varex Imaging Nederland B.V.Claymount — Varex Imaging Nederland B.V.Claymount — Varex Imaging Nederland B.V.Varex Imaging — Varex Imaging Nederland B.V.Claymount — Varex Imaging Nederland B.V.R-300 — SHIMADZU CORPORATIONClaymount — Varex Imaging Nederland B.V.Varex Imaging — Varex Imaging Nederland B.V.R-300 — SHIMADZU CORPORATIONRalco srl — RALCO SRLClaymount — Varex Imaging Nederland B.V.
Recent recalls
| Date | Firm | Reason |
|---|---|---|
| 2011-10-28 | Shimadzu Medical Systems | Shimadzu 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 |
| 2008-02-07 | Philips Medical Systems North America Co. Phillips | The collimator could fall from the x-ray stand, due to loosening screws, and strike a patient or operator underneath. |
| 2007-03-15 | Philips Medical Systems North America Co. Phillips | The Collimator field-defining light beam does not meet the light field contrast ratio requirement of 4:1. System is non-compliant with performance standard (102 |
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