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FDA 510(k)

MAGNETOM Terra; MAGNETOM Terra.X

K-Number: K232322 · 2024-03-22

ApplicantSiemens Medical Solutions USA, Inc.
Decision Date2024-03-22
Product CodeLNH
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

MAGNETOM Terra; MAGNETOM Terra.X is a medical device manufactured by Siemens Medical Solutions USA, Inc.. It received FDA 510(k) clearance on 2024-03-22 under approval number K232322. 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 Terra; MAGNETOM Terra.X?

MAGNETOM Terra; MAGNETOM Terra.X is a medical device that received FDA 510(k) clearance on 2024-03-22. It is manufactured by Siemens Medical Solutions USA, Inc.. The 510(k) number is K232322.

When was MAGNETOM Terra; MAGNETOM Terra.X approved by the FDA?

MAGNETOM Terra; MAGNETOM Terra.X received FDA 510(k) clearance on 2024-03-22, under approval number K232322.

What company makes MAGNETOM Terra; MAGNETOM Terra.X?

MAGNETOM Terra; MAGNETOM Terra.X is manufactured by Siemens Medical Solutions USA, Inc..

What is the FDA product code for MAGNETOM Terra; MAGNETOM Terra.X?

The FDA product code for MAGNETOM Terra; MAGNETOM Terra.X 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.

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