Ge Healthcare GmbH
Ge Healthcare GmbH holds FDA 510(k) medical device clearance, cleared in 2024, with 3 FDA device recalls on record.
Top product codes for Ge Healthcare GmbH
FDA recalls by Ge Healthcare GmbH
- Z-0935-2026 — GE HealthCare ViewPoint 6, Catalog Number H47601AA; Radiological image processing system
- Z-3146-2024 — ViewPoint 6, Model Numbers: a) H47581RJ, b) H47591MA, c) H47591MT, d) H47591PE, e) H47591PR, f) H47591RA, g) H47591SD, h) H47591YA; system, imaging processing, radiological
- Z-3145-2024 — ViewPoint; system, imaging processing, radiological
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 Ge Healthcare GmbH
Data sourced from openFDA. This site is unofficial and independent of the FDA.