MI View&GO
K-Number: K201202 · 2020-06-02
ApplicantSiemens Medical Solutions USA, Inc.
Decision Date2020-06-02
Product CodeLLZ
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 2020-06-02 under approval number K201202. The device is classified under product code LLZ. 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 2020-06-02. It is manufactured by Siemens Medical Solutions USA, Inc.. The 510(k) number is K201202.
When was MI View&GO approved by the FDA?
MI View&GO received FDA 510(k) clearance on 2020-06-02, under approval number K201202.
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 LLZ.
Other Devices by Siemens Medical Solutions USA, Inc.
Related Devices (Code: LLZ)
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.