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FDA 510(k)

SOFTWARE VERSION, D1.3 AND A1.3 FOR MAGNETOM

K-Number: K893640 · 1989-08-02

ApplicantSiemens Medical Solutions USA, Inc.
Decision Date1989-08-02
Product CodeLNH
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

SOFTWARE VERSION, D1.3 AND A1.3 FOR MAGNETOM 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 1989-08-02 under 510(k) number K893640. 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 SOFTWARE VERSION, D1.3 AND A1.3 FOR MAGNETOM?

SOFTWARE VERSION, D1.3 AND A1.3 FOR MAGNETOM is a medical device that received FDA 510(k) clearance on 1989-08-02. The listed applicant is Siemens Medical Solutions USA, Inc.. The 510(k) number is K893640.

When did SOFTWARE VERSION, D1.3 AND A1.3 FOR MAGNETOM receive FDA 510(k) clearance?

SOFTWARE VERSION, D1.3 AND A1.3 FOR MAGNETOM received FDA 510(k) clearance on 1989-08-02, under 510(k) number K893640.

Who is the listed applicant for SOFTWARE VERSION, D1.3 AND A1.3 FOR MAGNETOM?

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 SOFTWARE VERSION, D1.3 AND A1.3 FOR MAGNETOM?

The FDA product code for SOFTWARE VERSION, D1.3 AND A1.3 FOR MAGNETOM 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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