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FDA 510(k)

MRT 50A SOFTWARE RELEASE 9.0

K-Number: K900283 · 1990-03-19

ApplicantToshiba America Mri, Inc.
Decision Date1990-03-19
Product CodeLNH
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

MRT 50A SOFTWARE RELEASE 9.0 is the device name listed in this FDA 510(k) record. The listed applicant is Toshiba America Mri, Inc.. It received FDA 510(k) clearance on 1990-03-19 under 510(k) number K900283. 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 MRT 50A SOFTWARE RELEASE 9.0?

MRT 50A SOFTWARE RELEASE 9.0 is a medical device that received FDA 510(k) clearance on 1990-03-19. The listed applicant is Toshiba America Mri, Inc.. The 510(k) number is K900283.

When did MRT 50A SOFTWARE RELEASE 9.0 receive FDA 510(k) clearance?

MRT 50A SOFTWARE RELEASE 9.0 received FDA 510(k) clearance on 1990-03-19, under 510(k) number K900283.

Who is the listed applicant for MRT 50A SOFTWARE RELEASE 9.0?

The FDA 510(k) record lists Toshiba America Mri, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MRT 50A SOFTWARE RELEASE 9.0?

The FDA product code for MRT 50A SOFTWARE RELEASE 9.0 is LNH.

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Other records listing Toshiba America Mri, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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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