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FDA 510(k)

MRT-150A, MRT-150A SOFTWARE VERSION 11.9

K-Number: K941864 · 1995-01-26

Decision Date1995-01-26
Product CodeLNH
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

MRT-150A, MRT-150A SOFTWARE VERSION 11.9 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 1995-01-26 under 510(k) number K941864. 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-150A, MRT-150A SOFTWARE VERSION 11.9?

MRT-150A, MRT-150A SOFTWARE VERSION 11.9 is a medical device that received FDA 510(k) clearance on 1995-01-26. The listed applicant is Toshiba America Mri, Inc.. The 510(k) number is K941864.

When did MRT-150A, MRT-150A SOFTWARE VERSION 11.9 receive FDA 510(k) clearance?

MRT-150A, MRT-150A SOFTWARE VERSION 11.9 received FDA 510(k) clearance on 1995-01-26, under 510(k) number K941864.

Who is the listed applicant for MRT-150A, MRT-150A SOFTWARE VERSION 11.9?

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-150A, MRT-150A SOFTWARE VERSION 11.9?

The FDA product code for MRT-150A, MRT-150A SOFTWARE VERSION 11.9 is LNH.

Related Clinical Trials

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.

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.

View all 68 devices →

Related Devices (Code: LNH)

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.

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.

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