MAGNETOM Avanto Fit; MAGNETOM Skyra Fit; MAGNETOM Sola Fit; MAGNETOM Viato.Mobile— 510(k) K250443
Substantially EquivalentSiemens Healthcare GmbH
FDA 510(k) clearance K250443 for MAGNETOM Avanto Fit; MAGNETOM Skyra Fit; MAGNETOM Sola Fit; MAGNETOM Viato.Mobile, Substantially Equivalent on 2025-06-16. Applicant: Siemens Healthcare GmbH. Device class: 2.
Clearance details
- Applicant
- Siemens Healthcare GmbH
- 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
- Erlangen, DE
Recent devices under product code LNH
view allMore clearances from Siemens Healthcare GmbH
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 K250443
K-number listed on FDA's recall record- Z-2661-2025 — MAGNETOM Skyra fit. Model Number: 10849580.
- Z-2662-2025 — MAGNETOM Skyra Fit BioMatrix. Model Number: 11516217.
Matched by K-number from FDA's Recall Enterprise System record (openFDA device/recallk_numbers) — these recalls explicitly list K250443.
Data sourced from openFDA. This site is unofficial and independent of the FDA.