Magnetom Sola, Magnetom Altea and Magnetom Sola Fit
K-Number: K192496 · 2020-02-28
ApplicantSiemens Medical Solutions USA, Inc.
Decision Date2020-02-28
Product CodeLNH
Advisory CommitteeRA
DecisionSubstantially Equivalent
Device Summary
Magnetom Sola, Magnetom Altea and Magnetom Sola Fit is a medical device manufactured by Siemens Medical Solutions USA, Inc.. It received FDA 510(k) clearance on 2020-02-28 under approval number K192496. 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 Sola, Magnetom Altea and Magnetom Sola Fit?
Magnetom Sola, Magnetom Altea and Magnetom Sola Fit is a medical device that received FDA 510(k) clearance on 2020-02-28. It is manufactured by Siemens Medical Solutions USA, Inc.. The 510(k) number is K192496.
When was Magnetom Sola, Magnetom Altea and Magnetom Sola Fit approved by the FDA?
Magnetom Sola, Magnetom Altea and Magnetom Sola Fit received FDA 510(k) clearance on 2020-02-28, under approval number K192496.
What company makes Magnetom Sola, Magnetom Altea and Magnetom Sola Fit?
Magnetom Sola, Magnetom Altea and Magnetom Sola Fit is manufactured by Siemens Medical Solutions USA, Inc..
What is the FDA product code for Magnetom Sola, Magnetom Altea and Magnetom Sola Fit?
The FDA product code for Magnetom Sola, Magnetom Altea and Magnetom Sola Fit 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.