Siemens Medical Solutions USA, Inc., Ultrasound DI
Siemens Medical Solutions USA, Inc., Ultrasound DI has 0 FDA recalls, 0 inspections, 11 510(k) clearances and 0 compliance actions on record.
- Latest 510(k)
- Feb 9, 2017
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Summary
| Records | Count | Last refreshed | Source as of | Status |
|---|---|---|---|---|
| Recalls | 0 | Oct 23, 2026 | Not stated | Current |
| 510(k) clearances | 11 | Oct 4, 2026 | Not stated | Current |
| Inspections | 0 | Oct 27, 2026 | Not stated | Current |
| Compliance actions | 0 | Oct 23, 2026 | Not stated | Current |
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K163289 | syngo. CT Single Source Dual Energy (twin beam) | Feb 9, 2017 |
| K113179 | ACUSON SC2000 DIAGNOSTIC ULTRASOUND SYSTEM | Dec 7, 2011 |
| K112596 | ACUSON S2000 DIAGNOSTIC ULTRASOUND SYSTEM | Sep 16, 2011 |
| K081148 | SIEMENS ACUSON 2000 ULTRASOUND SYSTEM WITH ABVS TRANSDUCER | Dec 22, 2008 |
| K082142 | ACUSON S2000 DIAGNOSTIC ULTRASOUND SYSTEM | Nov 13, 2008 |
| K081121 | MODIFICATION TO ACUSON X150 ULTRASOUND SYSTEM | Jun 4, 2008 |
| K080760 | ACUSON X300 ULTRASOUND SYSTEM | Apr 25, 2008 |
| K072365 | SEQUOIA PLUS DIAGNOSTIC ULTRASOUND SYSTEM | Oct 17, 2007 |
| K072090 | SIEMENS DIAGNOSTIC ULTRASOUND SYSTEMS | Sep 14, 2007 |
| K071036 | MODIFICATION TO ACUSON X300 ULTRASOUND SYSTEM | May 16, 2007 |
| K063803 | ACUSON ANTARES DIAGNOSTIC ULTRASOUND SYSTEM | Jan 5, 2007 |