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FDA 510(k)

MAGNETOM 42 SP,63 SP,IMPACT

K-Number: K915112 · 1991-12-27

ApplicantSiemens Medical Solutions USA, Inc.
Decision Date1991-12-27
Product CodeLNH
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

MAGNETOM 42 SP,63 SP,IMPACT 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 1991-12-27 under 510(k) number K915112. 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 42 SP,63 SP,IMPACT?

MAGNETOM 42 SP,63 SP,IMPACT is a medical device that received FDA 510(k) clearance on 1991-12-27. The listed applicant is Siemens Medical Solutions USA, Inc.. The 510(k) number is K915112.

When did MAGNETOM 42 SP,63 SP,IMPACT receive FDA 510(k) clearance?

MAGNETOM 42 SP,63 SP,IMPACT received FDA 510(k) clearance on 1991-12-27, under 510(k) number K915112.

Who is the listed applicant for MAGNETOM 42 SP,63 SP,IMPACT?

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 42 SP,63 SP,IMPACT?

The FDA product code for MAGNETOM 42 SP,63 SP,IMPACT 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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