LUMINOS Q.namix T; LUMINOS Q.namix R— 510(k) K250660
Substantially EquivalentSiemens Medical Solutions
FDA 510(k) clearance K250660 for LUMINOS Q.namix T; LUMINOS Q.namix R, Substantially Equivalent on 2025-07-14. Applicant: Siemens Medical Solutions. Device class: 2.
Clearance details
- Applicant
- Siemens Medical Solutions
- Product code
- Code OWB
- Device class
- Class 2
- Regulation
- 21 CFR 892.1650
- Advisory panel
- Radiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Malvern, PA, US
Recent devices under product code OWB
view allMore clearances from Siemens Medical Solutions
view allAdverse events under product code OWB
product code OWB- Death
- 49
- Injury
- 340
- Malfunction
- 36,973
- Total
- 37,362
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 →
Recalls naming K250660
K-number listed on FDA's recall record- Z-1174-2026 — Interventional Fluoroscopic X-Ray System: LUMINOS Q.namix R; Siemens Material Number (SMN): 11574002; With Software Version VB10D-SP02
- Z-1175-2026 — Interventional Fluoroscopic X-Ray System: LUMINOS Q.namix T; Siemens Material Number (SMN): 11574003; With Software Version VB10D-SP02
Matched by K-number from FDA's Recall Enterprise System record (openFDA device/recallk_numbers) — these recalls explicitly list K250660.
Data sourced from openFDA. This site is unofficial and independent of the FDA.