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FDA 510(k)

SOFTWARE VERSION A2.5 FOR MAGNETOM 42SP/63SP SYST

K-Number: K924489 · 1993-01-15

ApplicantSiemens Medical Solutions USA, Inc.
Decision Date1993-01-15
Product CodeLNH
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

SOFTWARE VERSION A2.5 FOR MAGNETOM 42SP/63SP SYST 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 1993-01-15 under 510(k) number K924489. 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 A2.5 FOR MAGNETOM 42SP/63SP SYST?

SOFTWARE VERSION A2.5 FOR MAGNETOM 42SP/63SP SYST is a medical device that received FDA 510(k) clearance on 1993-01-15. The listed applicant is Siemens Medical Solutions USA, Inc.. The 510(k) number is K924489.

When did SOFTWARE VERSION A2.5 FOR MAGNETOM 42SP/63SP SYST receive FDA 510(k) clearance?

SOFTWARE VERSION A2.5 FOR MAGNETOM 42SP/63SP SYST received FDA 510(k) clearance on 1993-01-15, under 510(k) number K924489.

Who is the listed applicant for SOFTWARE VERSION A2.5 FOR MAGNETOM 42SP/63SP SYST?

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 A2.5 FOR MAGNETOM 42SP/63SP SYST?

The FDA product code for SOFTWARE VERSION A2.5 FOR MAGNETOM 42SP/63SP SYST 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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