MAGNETOM Vida, MAGNETOM Lumina, MAGNETOM Vida Fit— 510(k) K192924
Substantially EquivalentSiemens Medical Solutions USA, Inc.
FDA 510(k) clearance K192924 for MAGNETOM Vida, MAGNETOM Lumina, MAGNETOM Vida Fit, Substantially Equivalent on 2020-03-11. Applicant: Siemens Medical Solutions USA, Inc.. Device class: 2.
Clearance details
- Applicant
- Siemens Medical Solutions USA, Inc.
- Product code
- Code LNH
- Device class
- Class 2
- Regulation
- 21 CFR 892.1000
- Advisory panel
- Radiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Malvern, PA, US
Recent devices under product code LNH
view allMore clearances from Siemens Medical Solutions USA, Inc.
view allAdverse events under product code LNH
product code LNH- Death
- 11
- Injury
- 670
- Malfunction
- 1,460
- Other
- 2
- Total
- 2,143
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 K192924
K-number listed on FDA's recall record- Z-2658-2025 — MAGNETOM Lumina (DE). Model Number: 11344916.
- Z-2668-2025 — MAGNETOM Vida Fit. Model Number: 11410481.
Matched by K-number from FDA's Recall Enterprise System record (openFDA device/recallk_numbers) — these recalls explicitly list K192924.
Data sourced from openFDA. This site is unofficial and independent of the FDA.