Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in United StatesLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field., part of McKessonLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under 3 spellings of its name, each linked to the record.
As of Nov 15, 2026, FDA's public records list McKesson Medical Imaging with 5 device recalls and 3 510(k) clearances. The most recent is a device recall dated Dec 2, 2016: McKesson Radiology 12.2 - Picture Archive Communication System (PACS).
Drug approvals, 510(k) clearances, recalls and letters, 2017 to 2026 to date
A hatched bar is a year that is not over, so its count covers only part of the year.
| Dec 2, 2016 | McKesson Radiology 12.2 - Picture Archive Communication System (PACS)Class II · Issue for customers that use an EMR login or legacy web URL login or legacy web URL login for McKesson Radiology PACS th | Device recalls |
| Jan 6, 2015 | McKesson Radiology Mammography PlusK142850 · LLZ | 510(k) clearances |
| Jul 2, 2014 | MCKESSON RADIOLOGYK140909 · LLZ | 510(k) clearances |
| Jan 4, 2005 | HORIZON MEDICAL IMAGINGK043146 · LLZ | 510(k) clearances |
Spellings are joined only when they reduce to the same name, or a reviewed source names the same company. Sharing an FDA establishment number (FEI) is not enough: contract sites make products for many firms. Facts marked AI were labelled by a language model from the firm's FDA names; everything else comes from FDA or Wikidata. How this page is built
