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FDA 510(k)

MRT35-SP

K-Number: K905442 · 1990-12-21

ApplicantToshiba America Mri, Inc.
Decision Date1990-12-21
Product CodeLNH
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

MRT35-SP 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 1990-12-21 under 510(k) number K905442. 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 MRT35-SP?

MRT35-SP is a medical device that received FDA 510(k) clearance on 1990-12-21. The listed applicant is Toshiba America Mri, Inc.. The 510(k) number is K905442.

When did MRT35-SP receive FDA 510(k) clearance?

MRT35-SP received FDA 510(k) clearance on 1990-12-21, under 510(k) number K905442.

Who is the listed applicant for MRT35-SP?

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 MRT35-SP?

The FDA product code for MRT35-SP is LNH.

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.

K002531EXCELART WITH PIANISSIMO, MODEL MRT-1501/P3K002522OPART, MODEL MRT-600K000549OPART, MODEL MRT-600K993803EXCELART WITH PIANISSIMOK993574OPART/PRODIGA, OPART/PROTENZA, OPART/PARAGONK991740OPART, MODEL MRT-600

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Related Devices (Code: 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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