Siemens Medical Solutions USA, Inc. · Class II · Cleared Oct 30, 2024
| K-number | K243186 |
| Device name | Symbia Pro.specta Q3 (11364751); Symbia Pro.specta X3 (11364752); Symbia Pro.specta X7 (11364753); Symbia Pro.specta VA30A Family |
| Applicant | Siemens Medical Solutions USA, Inc. |
| Product code | KPS |
| Device class | Class II |
| Decision date | Oct 30, 2024 |
| Decision | Substantially Equivalent |
| Regulation | 892.1200 |
AI extraction for this record is queued and will appear within 24 hours. View full FDA record →
View the full FDA submission: accessdata.fda.gov