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FDA 510(k)

MAGNETOM Free.Max

K-Number: K210611 · 2021-07-01

ApplicantSiemens Medical Solutions USA, Inc.
Decision Date2021-07-01
Product CodeLNH
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

MAGNETOM Free.Max is a medical device manufactured by Siemens Medical Solutions USA, Inc.. It received FDA 510(k) clearance on 2021-07-01 under approval number K210611. 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 Free.Max?

MAGNETOM Free.Max is a medical device that received FDA 510(k) clearance on 2021-07-01. It is manufactured by Siemens Medical Solutions USA, Inc.. The 510(k) number is K210611.

When was MAGNETOM Free.Max approved by the FDA?

MAGNETOM Free.Max received FDA 510(k) clearance on 2021-07-01, under approval number K210611.

What company makes MAGNETOM Free.Max?

MAGNETOM Free.Max is manufactured by Siemens Medical Solutions USA, Inc..

What is the FDA product code for MAGNETOM Free.Max?

The FDA product code for MAGNETOM Free.Max 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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