MI View&GO
K-Number: K222172 · 2022-08-19
ApplicantSiemens Medical Solutions USA, Inc.
Decision Date2022-08-19
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 2022-08-19 under approval number K222172. 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 2022-08-19. It is manufactured by Siemens Medical Solutions USA, Inc.. The 510(k) number is K222172.
When was MI View&GO approved by the FDA?
MI View&GO received FDA 510(k) clearance on 2022-08-19, under approval number K222172.
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.
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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.