FDA 510(k) FDA class 2 Substantially Equivalent 🇩🇪 Germany

MAGNETOM Sola; MAGNETOM Altea; MAGNETOM Sola Fit; MAGNETOM Viato.Mobile; MAGNETOM Vida; MAGNETOM Lumina; MAGNETOM Vida Fit; MAGNETOM Flow.Elite; MAGNETOM Flow.Neo; MAGNETOM Flow.Rise

K Number: K252838 · Decision Dec 19, 2025
Classifications
1
FEI Numbers
146
Registration Numbers
146
Same Product Code
1098
Applicant Total
31
Review Days
105

Basic Information

Device Name
MAGNETOM Sola; MAGNETOM Altea; MAGNETOM Sola Fit; MAGNETOM Viato.Mobile; MAGNETOM Vida; MAGNETOM Lumina; MAGNETOM Vida Fit; MAGNETOM Flow.Elite; MAGNETOM Flow.Neo; MAGNETOM Flow.Rise
K Number
K252838
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.1000
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Siemens Healthcare GmbH
Date Received
September 5, 2025
Decision Date
December 19, 2025
Product Code
LNH
Advisory Committee
Radiology
Review Advisory Committee
RA
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
LNH System, Nuclear Magnetic Resonance Imaging

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K Number Device Name
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K253057 AI-Rad Companion Brain MR
K252608 AI-Rad Companion Prostate MR
K250443 MAGNETOM Avanto Fit; MAGNETOM Skyra Fit; MAGNETOM Sola Fit; MAGNETOM Viato.Mobile
K242551 syngo Dynamics (Version VA41D)
K242745 AI-Rad Companion Organs RT
K241770 Prostate MR AI (VA10A)
K240796 myAblation Guide (VB80A)
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