ACUSON S1000 / S2000 / S3000— 510(k) K132804
Substantially EquivalentSiemens Medical Solutions USA, Inc. Ultrasound Gro
FDA 510(k) clearance K132804 for ACUSON S1000 / S2000 / S3000, Substantially Equivalent on 2013-10-24. Applicant: Siemens Medical Solutions USA, Inc. Ultrasound Gro.
Clearance details
- Applicant
- Siemens Medical Solutions USA, Inc. Ultrasound Gro
- Product code
- Code IYN
- Advisory panel
- Radiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Moutain View, CA, US
Adverse events under product code IYN
product code IYN- Death
- 25
- Injury
- 163
- Malfunction
- 1,538
- Other
- 4
- Total
- 1,730
Source: openFDA MAUDE database, through . Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →
Data sourced from openFDA. This site is unofficial and independent of the FDA.