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Siemens Medical Solutions USA, Inc. Ultrasound Group

FDA Regulatory Profile

Siemens Medical Solutions USA, Inc. Ultrasound Group has 0 FDA recalls, 0 inspections, 3 510(k) clearances and 0 compliance actions on record.

Latest 510(k)
Feb 2, 2018

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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) clearances3Oct 4, 2026Not statedCurrent
Inspections0Oct 26, 2026Not statedCurrent
Compliance actions0Oct 23, 2026Not statedCurrent

Recent 510(k) Clearances

K-NumberDeviceDate
K173981ACUSON NX2 Diagnostic Ultrasound System, ACUSON NX2 Elite Diagnostic Ultrasound SystemFeb 2, 2018
K163635ACUSON S1000/S2000/S3000 Diagnostic Ultrasound SystemsJan 12, 2017
K152369ACUSON S1000, S2000, S3000 Diagnostic Ultrasuond SystemOct 6, 2015

FDA data resources