MAGNETOM Vida with syngo MR XA50A
K-Number: K213693 · 2022-02-25
ApplicantSiemens Medical Solutions USA, Inc.
Decision Date2022-02-25
Product CodeLNH
Advisory CommitteeRA
DecisionSubstantially Equivalent
Device Summary
MAGNETOM Vida with syngo MR XA50A is a medical device manufactured by Siemens Medical Solutions USA, Inc.. It received FDA 510(k) clearance on 2022-02-25 under approval number K213693. 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 Vida with syngo MR XA50A?
MAGNETOM Vida with syngo MR XA50A is a medical device that received FDA 510(k) clearance on 2022-02-25. It is manufactured by Siemens Medical Solutions USA, Inc.. The 510(k) number is K213693.
When was MAGNETOM Vida with syngo MR XA50A approved by the FDA?
MAGNETOM Vida with syngo MR XA50A received FDA 510(k) clearance on 2022-02-25, under approval number K213693.
What company makes MAGNETOM Vida with syngo MR XA50A?
MAGNETOM Vida with syngo MR XA50A is manufactured by Siemens Medical Solutions USA, Inc..
What is the FDA product code for MAGNETOM Vida with syngo MR XA50A?
The FDA product code for MAGNETOM Vida with syngo MR XA50A 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.