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FDA 510(k)

MRT-150 QD KNEE COIL

K-Number: K920096 · 1992-07-10

ApplicantToshiba America Mri, Inc.
Decision Date1992-07-10
Product CodeLNH
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

MRT-150 QD KNEE 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 1992-07-10 under 510(k) number K920096. 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-150 QD KNEE COIL?

MRT-150 QD KNEE COIL is a medical device that received FDA 510(k) clearance on 1992-07-10. The listed applicant is Toshiba America Mri, Inc.. The 510(k) number is K920096.

When did MRT-150 QD KNEE COIL receive FDA 510(k) clearance?

MRT-150 QD KNEE COIL received FDA 510(k) clearance on 1992-07-10, under 510(k) number K920096.

Who is the listed applicant for MRT-150 QD KNEE 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-150 QD KNEE COIL?

The FDA product code for MRT-150 QD KNEE COIL is LNH.

Other records listing Toshiba America Mri, Inc. as applicant

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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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