FDA Device Establishments · JSON-LD · Markdown
FEI 3002626007 · Develop Specifications But Do Not Manufacture At This Facility Manufacture Medical Device · Status: Active
| FEI Number | 3002626007 |
|---|---|
| Owner / Operator | SIEMENS MEDICAL SOLUTIONS USA, INC. (#9002915) |
| Address | 5168 Campus Dr., Plymouth Meeting, PA, US |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 6 |
| Product codes (top 20) | ITX, LLZ, IYO, OIJ, IYN, OBJ |
| Regulation § (21 CFR) | 892.1570, 892.2050, 892.1560, 892.1550, 870.1200 |
| Proprietary names | ACUSON S Family (S1000/ S2000 / S3000) Diagnostic Ultrasound System; ACUSON Freestyle Diagnostic Ultrasound System; ACUSON NX3 Diagnostic Ultrasound System; ACUSON Redwood Diagnostic Ultrasound System; ACUSON NX3 Elite Diagnostic Ultrasound System; ACUSON P500 Diagnostic Ultrasound System; ACUSON Sequoia Diagnostic Ultrasound System; ACUSON SC2000 Diagnostic Ultrasound System |
Source: openFDA. Public-domain (CC0).