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FDA 510(k)

MI View&GO

K-Number: K254016 · 2026-02-10

Decision Date2026-02-10
Product CodeQIH
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

MI View&GO is a medical device manufactured by Siemens Medical Solutions USA, Inc.. It received FDA 510(k) clearance on 2026-02-10 under approval number K254016. The device is classified under product code QIH. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MI View&GO?

MI View&GO is a medical device that received FDA 510(k) clearance on 2026-02-10. It is manufactured by Siemens Medical Solutions USA, Inc.. The 510(k) number is K254016.

When was MI View&GO approved by the FDA?

MI View&GO received FDA 510(k) clearance on 2026-02-10, under approval number K254016.

What company makes MI View&GO?

MI View&GO is manufactured by Siemens Medical Solutions USA, Inc..

What is the FDA product code for MI View&GO?

The FDA product code for MI View&GO is QIH.

Other Devices by Siemens Medical Solutions USA, Inc.

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Related Devices (Code: QIH)

Official Source

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