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iCAD, Inc.

Company NH
Found in 2 federal databases · 2 total records
fda 1 records
FDA Device Recall: DynaLOC Breast Interventional Planning Software Versions 3.1 and 3.2 2015-03-11
Class II — A device malfunction may cause the biopsy needle to fail to reach the intended target. If location confirming radiographs are not taken and properly evaluated, biopsy site mislocation can r...
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sec_efts 1 records
SEC Filing: ICAD INC 2024-03-29
SEC EDGAR filing — Forms: 10-K — Query: material event
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