MAGNETOM Skyra Fit
K-Number: K220589 · 2022-05-13
ApplicantSiemens Medical Solutions USA, Inc.
Decision Date2022-05-13
Product CodeLNH
Advisory CommitteeRA
DecisionSubstantially Equivalent
Device Summary
MAGNETOM Skyra Fit is a medical device manufactured by Siemens Medical Solutions USA, Inc.. It received FDA 510(k) clearance on 2022-05-13 under approval number K220589. 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 Skyra Fit?
MAGNETOM Skyra Fit is a medical device that received FDA 510(k) clearance on 2022-05-13. It is manufactured by Siemens Medical Solutions USA, Inc.. The 510(k) number is K220589.
When was MAGNETOM Skyra Fit approved by the FDA?
MAGNETOM Skyra Fit received FDA 510(k) clearance on 2022-05-13, under approval number K220589.
What company makes MAGNETOM Skyra Fit?
MAGNETOM Skyra Fit is manufactured by Siemens Medical Solutions USA, Inc..
What is the FDA product code for MAGNETOM Skyra Fit?
The FDA product code for MAGNETOM Skyra 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.