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FDA 510(k)

ADD'L SOFTWARE VERSION D2 FOR MAGNETOM 42 AND 63

K-Number: K901818 · 1990-05-23

ApplicantSiemens Medical Solutions USA, Inc.
Decision Date1990-05-23
Product CodeLNH
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

ADD'L SOFTWARE VERSION D2 FOR MAGNETOM 42 AND 63 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 1990-05-23 under 510(k) number K901818. 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 ADD'L SOFTWARE VERSION D2 FOR MAGNETOM 42 AND 63?

ADD'L SOFTWARE VERSION D2 FOR MAGNETOM 42 AND 63 is a medical device that received FDA 510(k) clearance on 1990-05-23. The listed applicant is Siemens Medical Solutions USA, Inc.. The 510(k) number is K901818.

When did ADD'L SOFTWARE VERSION D2 FOR MAGNETOM 42 AND 63 receive FDA 510(k) clearance?

ADD'L SOFTWARE VERSION D2 FOR MAGNETOM 42 AND 63 received FDA 510(k) clearance on 1990-05-23, under 510(k) number K901818.

Who is the listed applicant for ADD'L SOFTWARE VERSION D2 FOR MAGNETOM 42 AND 63?

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 ADD'L SOFTWARE VERSION D2 FOR MAGNETOM 42 AND 63?

The FDA product code for ADD'L SOFTWARE VERSION D2 FOR MAGNETOM 42 AND 63 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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