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FDA 510(k)

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 the device name listed in this FDA 510(k) record. The listed applicant is Siemens Medical Solutions USA, Inc.. It received FDA 510(k) clearance on 2022-04-01 under 510(k) 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. The listed applicant is Siemens Medical Solutions USA, Inc.. The 510(k) number is K220151.

When did MAGNETOM Avanto Fit receive FDA 510(k) clearance?

MAGNETOM Avanto Fit received FDA 510(k) clearance on 2022-04-01, under 510(k) number K220151.

Who is the listed applicant for MAGNETOM Avanto Fit?

The FDA 510(k) record lists Siemens Medical Solutions USA, Inc. as the applicant. This does not by itself establish the device manufacturer.

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.

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