MAGNETOM Avanto Fit
K-Number: K220151 · 2022-04-01
ApplicantSiemens Medical Solutions USA, Inc.
Decision Date2022-04-01
Product CodeLNH
Advisory CommitteeRA
DecisionSubstantially Equivalent
Device Summary
MAGNETOM Avanto Fit is a medical device manufactured by Siemens Medical Solutions USA, Inc.. It received FDA 510(k) clearance on 2022-04-01 under approval number K220151. 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 Avanto Fit?
MAGNETOM Avanto Fit is a medical device that received FDA 510(k) clearance on 2022-04-01. It is manufactured by Siemens Medical Solutions USA, Inc.. The 510(k) number is K220151.
When was MAGNETOM Avanto Fit approved by the FDA?
MAGNETOM Avanto Fit received FDA 510(k) clearance on 2022-04-01, under approval number K220151.
What company makes MAGNETOM Avanto Fit?
MAGNETOM Avanto Fit is manufactured by Siemens Medical Solutions USA, Inc..
What is the FDA product code for MAGNETOM Avanto Fit?
The FDA product code for MAGNETOM Avanto 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.