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FDA 510(k)

MRI SOFT TISSUE MOTION CORRECTION SOFTWARE VA10A

K-Number: K052305 · 2005-09-08

ApplicantSiemens Medical Solutions USA, Inc.
Decision Date2005-09-08
Product CodeLNH
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

MRI SOFT TISSUE MOTION CORRECTION SOFTWARE VA10A 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 2005-09-08 under 510(k) number K052305. 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 MRI SOFT TISSUE MOTION CORRECTION SOFTWARE VA10A?

MRI SOFT TISSUE MOTION CORRECTION SOFTWARE VA10A is a medical device that received FDA 510(k) clearance on 2005-09-08. The listed applicant is Siemens Medical Solutions USA, Inc.. The 510(k) number is K052305.

When did MRI SOFT TISSUE MOTION CORRECTION SOFTWARE VA10A receive FDA 510(k) clearance?

MRI SOFT TISSUE MOTION CORRECTION SOFTWARE VA10A received FDA 510(k) clearance on 2005-09-08, under 510(k) number K052305.

Who is the listed applicant for MRI SOFT TISSUE MOTION CORRECTION SOFTWARE VA10A?

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 MRI SOFT TISSUE MOTION CORRECTION SOFTWARE VA10A?

The FDA product code for MRI SOFT TISSUE MOTION CORRECTION SOFTWARE VA10A 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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