Dicom Grid, Inc.
Dicom Grid, Inc. holds FDA 510(k) medical device clearance, cleared in 2016, with 2 FDA device recalls on record.
Top product codes for Dicom Grid, Inc.
FDA recalls by Dicom Grid, Inc.
- Z-0941-2026 — Intelerad InteleShare software, with ProViewer component
- Z-1045-2017 — Ambra PACS UDI: +AMBRHEALTHSOLUTIONS0/$$+7_V3.16.13.0R Software Version Number: V3.16.13.0 Intended for use as a primary diagnostic and analysis tool for diagnostic images.
Recalls are matched by FDA's recalling-firm name — openFDA's enforcement dataset doesn't reference 510(k) numbers, so a recall here may cover devices beyond this company's 510(k) clearances.
Recent clearances by Dicom Grid, Inc.
Data sourced from openFDA. This site is unofficial and independent of the FDA.