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Ge Medical Systems Ultrasound And

FDA Regulatory Profile

Ge Medical Systems Ultrasound And has 0 FDA recalls, 0 inspections, 5 510(k) clearances and 0 compliance actions on record.

Latest 510(k)
Jul 22, 2022

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Summary

Record counts and when each FDA source was last refreshed
RecordsCountLast refreshedSource as ofStatus
Recalls0Oct 23, 2026Not statedCurrent
510(k) clearances5Oct 4, 2026Not statedCurrent
Inspections0Oct 25, 2026Not statedCurrent
Compliance actions0Oct 23, 2026Not statedCurrent

Recent 510(k) Clearances

K-NumberDeviceDate
K220882Vivid E80, Vivid E90, Vivid E95Jul 22, 2022
K200708Vivid iqSep 9, 2020
K200743Vivid E80/ Vivid E90/ Vivid E95Jul 23, 2020
K200138Versana PremierJul 1, 2020
K192917ViewPoint 6Jan 6, 2020

FDA data resources