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FDA 510(k)

MRT-50 QD HEAD COIL

K-Number: K920097 · 1992-03-31

ApplicantToshiba America Mri, Inc.
Decision Date1992-03-31
Product CodeLNH
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

MRT-50 QD HEAD COIL 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 1992-03-31 under 510(k) number K920097. 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-50 QD HEAD COIL?

MRT-50 QD HEAD COIL is a medical device that received FDA 510(k) clearance on 1992-03-31. The listed applicant is Toshiba America Mri, Inc.. The 510(k) number is K920097.

When did MRT-50 QD HEAD COIL receive FDA 510(k) clearance?

MRT-50 QD HEAD COIL received FDA 510(k) clearance on 1992-03-31, under 510(k) number K920097.

Who is the listed applicant for MRT-50 QD HEAD COIL?

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-50 QD HEAD COIL?

The FDA product code for MRT-50 QD HEAD COIL 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.

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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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