Intelerad Medical Systems Incorporated
Intelerad Medical Systems Incorporated holds FDA 510(k) medical device clearances, first cleared 2009, most recent 2020, with 2 FDA device recalls on record.
Top product codes for Intelerad Medical Systems Incorporated
FDA recalls by Intelerad Medical Systems Incorporated
- Z-0723-2026 — IntelePACS - InteleConnect / TechPortal
- Z-1208-2025 — IntelePACS (Image Fusion Module) - InteleViewer
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 Intelerad Medical Systems Incorporated
Data sourced from openFDA. This site is unofficial and independent of the FDA.