Ge Vingmed Ultrasound AS
Ge Vingmed Ultrasound AS holds FDA 510(k) medical device clearances, first cleared 2009, most recent 2015, with 6 FDA device recalls on record.
Top product codes for Ge Vingmed Ultrasound AS
FDA recalls by Ge Vingmed Ultrasound AS
- Z-2317-2024 — GE Vivid Ultrasound products, Model Numbers: a) Vivid S70, H45041SW
- Z-2316-2024 — GE Vivid Ultrasound products, Model Numbers: a) Vivid E90, H45581LB; b) Vivid E95, H45581DA
- Z-2127-2023 — GE Healthcare Vivid S70N, ultrasound device
- Z-2126-2023 — GE Healthcare Vivid S60N, ultrasound device
- Z-2124-2023 — GE Healthcare Vivid S60, ultrasound device
- Z-2125-2023 — GE Healthcare Vivid S70, ultrasound device
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 Vingmed Ultrasound AS
- K150087 — Vivid E80 Diagnostic Ultrasound Imaging System, Vivid E90 Diagnostic Ultrasound Imaging System, Vivid E95 Diagnostic Ultrasound Imaging System
- K150085 — GE EchoPAC
- K141093 — 6VT-D ULTRASOUND TRANSDUCER
- K131685 — GE ECHOPAC
- K131514 — GE VIVID E9 DIAGNOSTIC ULTRASOUND IMAGING SYSTEM
- K123894 — GE ECHOPAC
- K120201 — GE VIVID E9 DIAGNOSTIC ULTRASOUND IMAGING SYSTEM
- K101149 — GE VIVID E9 DIAGNOSTIC ULTRASOUND IMAGING SYSTEM
- K101324 — GE ECHOPAC MODEL BT10
- K092756 — GE VSCAN COMPACT DIAGNOSTIC ULTRASOUND SYSTEM
Data sourced from openFDA. This site is unofficial and independent of the FDA.