FDA 510(k)

NON-UNIFORM ATTENUATION CORRECTION SYSTEM

K-Number: K942145 · 1995-02-22

ApplicantSiemens Medical Solutions USA, Inc.

Decision Date1995-02-22

Product CodeKPS

Advisory CommitteeRA

DecisionSubstantially Equivalent

Device Summary

NON-UNIFORM ATTENUATION CORRECTION 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 1995-02-22 under 510(k) number K942145. The device is classified under product code KPS. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NON-UNIFORM ATTENUATION CORRECTION SYSTEM?

NON-UNIFORM ATTENUATION CORRECTION SYSTEM is a medical device that received FDA 510(k) clearance on 1995-02-22. The listed applicant is Siemens Medical Solutions USA, Inc.. The 510(k) number is K942145.

When did NON-UNIFORM ATTENUATION CORRECTION SYSTEM receive FDA 510(k) clearance?

NON-UNIFORM ATTENUATION CORRECTION SYSTEM received FDA 510(k) clearance on 1995-02-22, under 510(k) number K942145.

Who is the listed applicant for NON-UNIFORM ATTENUATION CORRECTION 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 NON-UNIFORM ATTENUATION CORRECTION SYSTEM?

The FDA product code for NON-UNIFORM ATTENUATION CORRECTION SYSTEM is KPS.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.