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FDA 510(k)

MAGNETIC RESONANC DVCE VISART V 3.5 SOFTWARE

K-Number: K965068 · 1997-07-15

ApplicantToshiba America Medical Systems, In.C
Decision Date1997-07-15
Product CodeLNH
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

MAGNETIC RESONANC DVCE VISART V 3.5 SOFTWARE is the device name listed in this FDA 510(k) record. The listed applicant is Toshiba America Medical Systems, In.C. It received FDA 510(k) clearance on 1997-07-15 under 510(k) number K965068. 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 MAGNETIC RESONANC DVCE VISART V 3.5 SOFTWARE?

MAGNETIC RESONANC DVCE VISART V 3.5 SOFTWARE is a medical device that received FDA 510(k) clearance on 1997-07-15. The listed applicant is Toshiba America Medical Systems, In.C. The 510(k) number is K965068.

When did MAGNETIC RESONANC DVCE VISART V 3.5 SOFTWARE receive FDA 510(k) clearance?

MAGNETIC RESONANC DVCE VISART V 3.5 SOFTWARE received FDA 510(k) clearance on 1997-07-15, under 510(k) number K965068.

Who is the listed applicant for MAGNETIC RESONANC DVCE VISART V 3.5 SOFTWARE?

The FDA 510(k) record lists Toshiba America Medical Systems, In.C as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MAGNETIC RESONANC DVCE VISART V 3.5 SOFTWARE?

The FDA product code for MAGNETIC RESONANC DVCE VISART V 3.5 SOFTWARE 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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