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FDA 510(k)

MAGNETOM TRIO A TIM SYSTEM

K-Number: K050200 · 2005-02-28

ApplicantSiemens Medical Solutions USA, Inc.
Decision Date2005-02-28
Product CodeLNH
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

MAGNETOM TRIO A TIM SYSTEM 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 2005-02-28 under 510(k) number K050200. 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 TRIO A TIM SYSTEM?

MAGNETOM TRIO A TIM SYSTEM is a medical device that received FDA 510(k) clearance on 2005-02-28. The listed applicant is Siemens Medical Solutions USA, Inc.. The 510(k) number is K050200.

When did MAGNETOM TRIO A TIM SYSTEM receive FDA 510(k) clearance?

MAGNETOM TRIO A TIM SYSTEM received FDA 510(k) clearance on 2005-02-28, under 510(k) number K050200.

Who is the listed applicant for MAGNETOM TRIO A TIM SYSTEM?

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 TRIO A TIM SYSTEM?

The FDA product code for MAGNETOM TRIO A TIM SYSTEM 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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