MAGNETOM AVANTO-FIT, MAGNETOM SKYRA-FIT— 510(k) K130885
Substantially EquivalentSiemens Medical Solutions USA, Inc.
FDA 510(k) clearance K130885 for MAGNETOM AVANTO-FIT, MAGNETOM SKYRA-FIT, Substantially Equivalent on 2013-05-17. 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
- Martinez, CA, 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 K130885
K-number listed on FDA's recall record- Z-2661-2025 — MAGNETOM Skyra fit. Model Number: 10849580.
- Z-0467-2016 — MAGNETOM systems, magnetic resonance diagnostic devices (MRDD).
Matched by K-number from FDA's Recall Enterprise System record (openFDA device/recallk_numbers) — these recalls explicitly list K130885.
Data sourced from openFDA. This site is unofficial and independent of the FDA.