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FDA 510(k)

DIFFUSION WEIGHTED MR IMAGING /MAGNETOM VISION

K-Number: K971055 · 1997-06-20

ApplicantSiemens Medical Solutions USA, Inc.
Decision Date1997-06-20
Product CodeLNH
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

DIFFUSION WEIGHTED MR IMAGING /MAGNETOM VISION 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 1997-06-20 under 510(k) number K971055. 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 DIFFUSION WEIGHTED MR IMAGING /MAGNETOM VISION?

DIFFUSION WEIGHTED MR IMAGING /MAGNETOM VISION is a medical device that received FDA 510(k) clearance on 1997-06-20. The listed applicant is Siemens Medical Solutions USA, Inc.. The 510(k) number is K971055.

When did DIFFUSION WEIGHTED MR IMAGING /MAGNETOM VISION receive FDA 510(k) clearance?

DIFFUSION WEIGHTED MR IMAGING /MAGNETOM VISION received FDA 510(k) clearance on 1997-06-20, under 510(k) number K971055.

Who is the listed applicant for DIFFUSION WEIGHTED MR IMAGING /MAGNETOM VISION?

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 DIFFUSION WEIGHTED MR IMAGING /MAGNETOM VISION?

The FDA product code for DIFFUSION WEIGHTED MR IMAGING /MAGNETOM VISION 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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