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FDA 510(k)

MAGNETOM Viato.Mobile

K-Number: K240608 · 2024-03-29

ApplicantSiemens Medical Solutions USA, Inc.
Decision Date2024-03-29
Product CodeLNH
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

MAGNETOM Viato.Mobile is a medical device manufactured by Siemens Medical Solutions USA, Inc.. It received FDA 510(k) clearance on 2024-03-29 under approval number K240608. 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 2024-03-29. It is manufactured by Siemens Medical Solutions USA, Inc.. The 510(k) number is K240608.

When was MAGNETOM Viato.Mobile approved by the FDA?

MAGNETOM Viato.Mobile received FDA 510(k) clearance on 2024-03-29, under approval number K240608.

What company makes MAGNETOM Viato.Mobile?

MAGNETOM Viato.Mobile is manufactured by Siemens Medical Solutions USA, Inc..

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

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

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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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