FDA Device Establishments · JSON-LD · Markdown
FEI 3023245 · Complaint File Establishment per 21 CFR 820.198 Develop Specifications But Do Not Manufacture At This Facility Manufacture Medical Device · Status: Active
| FEI Number | 3023245 |
|---|---|
| Owner / Operator | SIEMENS MEDICAL SOLUTIONS USA, INC. (#9002915) |
| Address | 22010 S.E. 51ST ST., ISSAQUAH, WA, US |
| Registration expiry | 2026 |
| Initial importer flag | Y |
| Registered products | 6 |
| Product codes (top 20) | IYN, IYO, ITX, QIH, OIJ, OBJ |
| Regulation § (21 CFR) | 892.1550, 892.1560, 892.1570, 892.2050, 870.1200 |
| Proprietary names | ACUSON Sequoia Diagnostic Ultrasound System; ACUSON Sequoia Select Diagnostic Ultrasound System; ACUSON Origin Diagnostic Ultrasound System; ACUSON Origin ICE Diagnostic Ultrasound System |
Source: openFDA. Public-domain (CC0).