Intelerad Medical Systems Incorporated
Intelerad Medical Systems Incorporated holds FDA 510(k) medical device clearances, first cleared 2009, most recent 2020, with 3 FDA device recalls on record.
Top product codes for Intelerad Medical Systems Incorporated
FDA recalls by Intelerad Medical Systems Incorporated
- Z-0186-2027 — IntelePACS, InteleConnect Portal/Tech Portal Versions PACS-5-1-1-R102, PACS-5-2-1-R93, PACS-5-3-1-R83 through R128, PACS-5-4-1-R66 through R101, PACS-5-5-1-R50 through R89, PACS-5-6-1-R41 through R81, PACS-5-7-1-R21 through R61, PACS-5-8-1-R2 through R42, PACS-5-9-1-R8 through R19; System, Image Processing, Radiological
- 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.