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FDA 510(k)

MAGNETOM Viato.Mobile

K-Number: K232482 · 2023-09-06

ApplicantSiemens Medical Solutions USA, Inc.
Decision Date2023-09-06
Product CodeLNH
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

MAGNETOM Viato.Mobile is the device name listed in this FDA 510(k) record. The listed applicant is Siemens Medical Solutions USA, Inc.. It received FDA 510(k) clearance on 2023-09-06 under 510(k) number K232482. The device is classified under product code LNH. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MAGNETOM Viato.Mobile?

MAGNETOM Viato.Mobile is a medical device that received FDA 510(k) clearance on 2023-09-06. The listed applicant is Siemens Medical Solutions USA, Inc.. The 510(k) number is K232482.

When did MAGNETOM Viato.Mobile receive FDA 510(k) clearance?

MAGNETOM Viato.Mobile received FDA 510(k) clearance on 2023-09-06, under 510(k) number K232482.

Who is the listed applicant for MAGNETOM Viato.Mobile?

The FDA 510(k) record lists Siemens Medical Solutions USA, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MAGNETOM Viato.Mobile?

The FDA product code for MAGNETOM Viato.Mobile is LNH.

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Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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